SCIENTIFIC ABSTRACT GRIGOREVA, N.E. - GRIGORYEVA, T.G.

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SCIENTIFIC ABSTRACT
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Web m E. Grigar eVai-PPI abzkch. tm-' 107-111),- T%u ncw pe~ntamrthjn' 'J,i~l were prepurd, vit chlorOu M I py,idu'o WE of 2 -dinitr4 I'dr,,chla-idm of p pf--n,-ut r!, i- In alk111fir aledia lt~' 'h-fij'~Ut t'% of thc%~ dyes was d~!ccrrnuirfj in ~,]%~ents in ttle - t NaOH. HCI, HOA, and ff,CO, S~rritnctrt-l ~t~t. I "kn'i As~Avc in Nfe and Et alriihok , tt,ry di4~ivv fjj~,rr ~fj KIr'. '.. arctic acid and 0&11&0 to reddiiih-violet colours &iruil4r to th-, d bcnzidiite der.-. hi pft~Ftnco of Rkubol (but differ in thAt b~' of the solution the colour i1cepens). Max. otrad min vary rording to strength of solution, &W-aptiou I.j%-cr in acett, acid L~irkg five timm higher than in alcoholl + HCL Max. abs."ption of nionokaits U in F-tOH is 465 m0a and in acctono 495 ni~L am Thoteric nature is shown by formation L;f ctiloured salts witla acids a alkalis. Cations acid aniont in alcohol cidubit gamilar colouri (max. absirption 630 tniA.). Aniows colouri exhibit more statmtlity thAtI cAtivas- A 1, B 14~mtilllt 5.2 K; ili pymliii~mi) (1) ";it[' -1 14~ !'-Oll! It) nti.-. g:;v- :; d4tk W141 N11c,CQ Idt b~ldn-t. lipt . wid, 11 101cr r-iihinlc Avith 1110 tMorid,, dark-ml, tit. 167' (conlaius 0.5 V-011 ), fr Which fiwt.ry cr-stii. qolvct cauld nct be foimd. 11cating to*-L~"4'33' in 11(1I1fl1Ttari!m of %uric Tonoval of t1m. latfrr with III)( Me-(-O plye a litw-vyl r,4111t, which 00,ki-I 60"o (f-IJCoTf,Nll,)CI (111), Ycilow (Irmn M )I J_ -A01f; M10). U1. Whi0i CGMAHC(l 0,46 MCAC 1. L Or"'Itc, YCHOW, M. (fr,m EtOlf and IGO). I (I g.) ruid 1,3 g. 111( CI ,aft litatvill In 5 ml, ELUI I aud 2 ial. pyr- 15 -11hi. (.11 stvain O.-oll gave n Ictl i?Ft. (initially violtf ). which aftrr wa0iinj wa4 chriffilt(igTA11hf-ji rin Allot yiddi,g grccri Nill twl.sll : C1101; ClICH: in.21.ul'x Eo*,5~,1,4(ift~)11),Fg:l~)(1--tf)tl.flc)),(*.t)if(fl(:(),11), lt~fluxuj 18ith pYlidine I hr., filtt:tcd an(I evapl. tjjjj ~,jvc Some diuitruaniline and lit, is(ilatc(I as the ploatc, wa:;1:iujr 'the imidile with ]Is( ) gave rin uuidentiriL-d git:t-n pr-Auct, Ilcut-ing L with P-Csl(,(NITAc)t I,% I"toll r)51,',j (RI. (M. It , - P-L.1411. C4114). vicilct, tit. 147' (tx(,tn Acoll), 'AtLiCII J1CjtC(I t0 itj ul-p- and treated wit), 11,0 gave In, "7&-7* (from Ftoll-l~y)); fj(rrj#, ;,cjjnjv, in, I I rind gave 671J10 vi.,-Iet IV (it, - p. Afr,NC7,1lj, it, IIII Mom Etolf) 1101 Imited Willi 11,0 Y T 7-7-77 - - g ?'A~ Qlx~ V m fill., I lQI salt ht aled with Nal. it I Pvc Ptr-n decomp, 2-10" x (Clixj)" 41~0 4-du (I't0m. Mir-)und 1.15 g. III licatud 5 mics, fit EtOIr' (reat(A Ivith I till. pytidine aud licatui until I Itut reacted (2 Ill-1.) g-Ave 0.0 jr. orange-reA solid, which repptd. (viiii EtOlf with Me'lZO j"-J%c Pate YLIlow in. 2&r)* (from EtOll-Etco) (COntnilli 1,25 Illolr:q 11tOll); pirra.e, Ill. 233': 1 f, 23 ;;.) in 1-4011 Imited Willi IS g. m-CJ1 00 0.5 fir. g ive 11) g~ n-rud 11' Oz I - Ill, ) tUilli 2 UPACq IWO11); lXAtCfj W IS2' (0 ill- ci llmt m it gave'4 Innivit Will which 19:41 pa-:;td over A, Os In EtOlt and file, effluent roln. tr,-.Ited with EtIO. yielding a brown !:nI3A, in, 22~18', it compd. of 2 ril"Icl On. Iwjr 1 Nlf,)CI (VI) mid I tw4c di.-Onior wiih 2 )~tol(,* file rLitfuat 'suln' trc-mUl With tll11ZC E'lvc ytll~AV vitvdieg ~,f V1, m, 715" 0,j mc-1z: E1011). I J.'.) awl I g. in 1`1011 11C.-Itcd 3 mir). kpv~! 0.2 ain;ust black IV i-j1lNCJJ',), m. 160'. If fl.e' I e, gf:llti w(.--le lliA ill jorl :3 i~' rty., lilld 11f.it(A 21) til~ll. In F(011' tl~~Lrc! f'-tiv"I 0.:1 r. ,nr"-~n (Olive- c.11'xil (.1(: 61 ('11., OU CH., "'71 ( 1, 22-3, ONI&II lct~lills I'A IfJO); tht-l-111,11 p,;ivv, di- liltn"Illilille alid a vit, 'llik, b~AIZ11j''Ic &~V' ."I glut.1"s'll- a)(Ithyde wasdecol."l;f), (cf. Twymr-;,rlal- C.A.49. 102,~~M) nxid 2A g. ci( the yel (jw jjv-uii(-t vvwi tak-en tit, in hot txiLA. IICJ; (M COCIiilr fill! R0111. %Vi n1'(ltMIi1C(I lNitli N11,Off, Ykidiug yellow lit. 307' ~frwn EtOlf), which has 1 14111, Laoilp uv~iikiblc f~,r dia;r-tmiti-n. lhi3 (0.5 g.) und 0.5 r. I ImattA in Elf) I with 2 jul. pyri-Jine 15 inin. and kept 12 Ins. i-~ivc 517c, IN IV IR' - (P-kC, 11,101, which does not rr.(It. but (Icktimp. na licaling, the product, C61I.N.Ch. cc;ntains 3 tr-le.,4 FtOll. Thu4 im- vLb~.tivitul di. alims Can mlvt with quMcmary pyriditlit'sn salt:i in 1, 1: 1,,uid 1:2 plipotti,mi. G,- M. C' 'A X I) Influms of And 211tatiles WiribitaItion qlrcl ytkUnG 4yel. V. 9, Ortpit'itin. 1. K. lkwl A. et", state Unlv,, Kharkov). zhftr~ ObAthel Vim. 3(W1 103);, d. CA. 00, 13778b.-AW)rptiou ~Wtm I a-base dye$ Won txmnid. In 0% EtQif,-- aw SM 'Ith varybig arnts. of NO. L'Or tic AcOf I; 7 tpoctra wcrttxamd.al&oInak.,.&Wna. with varying un . of NOR- The pytidina d t In Aq. RLOH Undergo hydmlydi whkh Is more httet= Teases of comp(li. w;th I any acid added tothe saln. shifts Ww" basicity of the ~atlion. the equil. In the direction of the dye salt while alkali shift. .,tho equil. in th* dirretion (A the but 11 the dye containsi -40nor 'groupti; with elect mn-acrept of FT(JUP3 the afti. of alkah ylelfb del-Ply--colomd "losic dyt,3. The Anilintsime pplilim.- t1v;:_s are dreoloriztcl In concd, 14904 ovylu to salt romiAtion, thc~e to the oflj~lnltf dYN -6. max. ime noled la M01 I atil ots d4n. The following at EtO14 with excess HCI# resp., for the following dyti of type RN11(CH)11:NHRCl (R thown): Ph, 485 Eng, 495 injA; p- C MeWlil 495 495; PO&OCJ14 600. &)U; P-HOUlt 105, 805; -1-Cilli, 410, 480, 2-C!,Jl, i~2, 550; p-OtNCjjH,41U~-b27, Thevarlowtivpermauze reptoduced. frotiii excm NaO11 and pyridine-SO.) with"p- 14MIllautoll,inthe rivencerifa. little 11C[gave Z JjCj,yjo1tt,m, '4C3-4*,whld%rttainsrtO1f. 4 6t fVtd104 a 01kounit with a 1. K. Waite &ud N. G.' swt tw Joy, zim o1). z1of. 6SACM xh~m IGNI ' ef. Ud#MY* Z4VIA4 Kkof,im C303%. ic'd. Vah.- so, IAllat wai pudftj by tstattgent with CUSC44 and With m Kt. of phttal c co vetk arthrdsides reflIL", a on. Thu Pkire m-At H'11' b. 144*. pictste, to. W. Aals (2.15 tztl,) and 1.5 C. 2,4-di- 13 keobcmzm* (1) heated briefly to forra a sain., thm ~Itd~o With W ML 4!7 r240 And k4rVt I 41AY yiddi If IM compmeit-1 sr4 hented & hin. it to,, the $AMC poduct foctmA. 71le Salt, treuOd with 15% Mail, 'the red "V~417 of lot* ". memm HtAttag the t with '.t, I't ntnex In E Wit at 5"0* tare an vptp.~ with 9 1IC1 the CmT"Ppad. 8.4 ~~sNHAP Ai show-1:1 A, md-bmwn, m. blts;~IM, . 130-, ), 493, In the prera. of It j'%t*TsthtmaWf&me4 viokc 4 3tlhint tile (tunt thero- 611ne'. thip rabnUnre "on,of 11 W" P tM41: S.27R, V W j"'Y'a-042,60,M. 167, (from keoll), cc at. OP. (tratri MftCO), this pawed over A" give an Upp" 1110W %=e to", aW lawtr Yk4et The Latter Outod *itb 36 cjCG Cave tb4 Pam M yeseg" h led ovc, P.O. at 7so I 121 0. deep AoW, ~m~ I hr. t shve sum I to t. and sayt purt Cjj1W- 04NsC7, a dark &Q). 7ne yellow chronuk(cVaphic zo:ir, ab~n tat 1 Y -T 6 in o pe" C=P. 'd WAII 'i Ul. lk Utae courpo"d, lnfu*ib:o omd gpf I was t!so d%ved tyadtua A= T. 1, 71 spwtTaly Morl, U E and p 44 v, 4-dWtpiila-rvhwy at 130%. 111 W" JJCOH j-ATt I dt4CP tj~~.d flgd aq trtatraut vrtt!3 4 Meoll Ngalt PYO a Mut Oka Cal. odftq IV WIA a- r41T4N:Clfcy(:cl(cl.f;Cfiw: ---------- Distr: hF-hJ/hE3d "COMIU4 hydr4-tn *103 of N- I substitutO4 Inid i n !~~-CT M - ;' R Gjjr-Z;va, A. ov) f. mjkAel ry yridinimn dskyr-Wej were lgel-d. amirding to Vacke MI. 329(1(X)4)) wiOuKa tiols by boatits pylidin'! omitirs in FtOH f,)Iuwrd by dign. cA RtOlf and ht-Atinj thr, millne with 1110 wit the dy-a was dinitmanifine --I --cmkm~; tt~rti a Om fvltratc~ with EW Anp trtatsurnt wilh C. Nval e, j-'J. to ykld zfe ck-wircl arylpyTidLaium :111cride. I I y&og 11tv't- tion ot pyridist &kooSAmnylmtc in MvOll ovct Ft%. gave M-PAOM piperUine IRT gal, M. 2w'. 'wife-m Similaarly, Tim &btai"-d:_4 11-C-3 F44, 171A Hcl 110 sau. W, a 11 1 GAU coll)d Dm it Vwifiej, f(rdromation, of tht lict %sit ci Which dw fKt cr-'at; thih with V40H w0 'V-f"4mfq'*1-! YiY?j4t4FWU, Ell, I I G. M. KQwJ&wj GRIGORIYEVA, N.Ye. 1% -Mmwmw~ Pentatueth=(P~ridins) dyes. Uch. zap. KIIGU 95:207-230 '57. (MIRA 12:10) (Pyridine) (Vfes and dyeing) GRIGORIYIVA, R.Ye. Catalytic activity of diatomite. Bent. gliny Ukz. no.2:136-140 158. (MIRA 12:12) 1.Kharlkovokly gosudarstvenW univerettet. (Catalysts) (Diatomite) AUTHORS: Gri--orlyeva, ff. Yo., Foch!~a, A. A, juv/79-26-6-54/63 TITLE: Morjoanils of Glutaconedialde~$iyde (Monoanily ~:lutakonoyogo dialldoC;Jda) I. Derivatives of Pri:nary Aromatic Aninos (I. Proizvo(Inyyo porvichnykh aronatichenkikh aminoy) PERIODICAL: Zhurnal obnhchey khimii, 1958, Vol. 26, Itr 6, pp. 1677 - 16C1 (USSR) ABSTRACT: Of the derivatives of prinary anines only the dinitro-subutituted ones were known (Rof 1). One of the authors _-..nthetized the correoponding anilinederivatives anti other primary aromatic amines (Refs 4,5)- However, the nature of these com;~ounda was not in- vesti~:ated in detail as their yields were toonmall. In order to investiEate similar compounds more clocely the authors elabo- rated a method of synthesis of '%-.he derivatives of aniline and of other aminee; in some cases they obtained conoi!erable yields, and the authors could inverti~.:ate their condensability with aro- matic amines and compounds containin- active methyl 6-roups. The condensation of the monoanilo with aromatic amines was carried out under different co,ditions: in acetic acid in the presence of hydrochloric acid, in acetic --nhydride in t"'e presence of Card 1/3 hydrogen chloride and in pyridine in the prenence of hydrogen Monoanilo of Glutnconedialdehyde. 1. Darivativev of JUV/79-26-6-54/63 rri;;,"ry Aromatic Amines chloride. Only in the lnut mentioned case a color chwire occurrel, which could bo t~,)-en as an indication as to the nature of the process of reaction, howevor, no definite reoult could be achieved, The invozti--.-~tions c.,rriud out of the monoanils of glutacone uldehydo ahowod in any way that they are of ampho- teric character. Their conde-aability with comWoundu haying active Met*1 droupo can nerye as indirect proof of the strlicture of thqobtained monoanils. Thus the monoanils of glutacone alde- hyde are investigated as derivatives of aromatic amines. It was shown that the unsubstituted monoanil and the monoanils of glutacone aldehyde with nucleophilic substituents in the aro- matic nuclei do not enter the condensation with aromatic amines. The condensation of some monoanils with the methiodide of 2-.-.iethylbenzthiazole was carried out, however, the structure of the initial products could not be determined. There are 2 tables and 9 references, 3 of which are Soviet. Card 2/3 Monoanils of Glutaconedialdehyde. 1. Derivatives of 30V/79-26-6-54/63 Primary Aromatic Anines ASSOCIATION: KharIkovskiy gosudarstyennyy universitet (Kharlkov State University) SUBMITTED: May 12, 1957 1. Aniline derivatives--Synthesis Gard 3/3 AUTHO'AS: GriCorlyevat H. Yo., Gintse, I. K. .30-1/79-28-6-55/63 TITLE: - -ro-h-o-anila of G1_u_taoLm Aldehyde (Monoanily glutakonoyogo dir-11- dej;ida) II. The Influe~ce of the Mediu~m on tle Color of the De- rivatives of Primary Aromatic Amines (II. Vliyaniye sredy na okrauc% proizvodnyl:h pervichnykh aromatiche3kikh aminov) PERIODICAL: Zhurnal obahchey khimii, 1958, Vol. 28, Hr 6, pp. 1682 - 1689 (USSR) ABSTRACT: The problem concerning the influence of tl.e medium on '..'a color of the organic compounds has interested scientinto already since long. The unualty intraionoic dyes are especially sensitive to changes of the nedium. Many hypotheses have already been suegested for thin problem (Refs 1-5). That by Kiprianov and his colla- boratorn is widely acknowledt;ed (Ref 6) as are those by other authors (Ref 7) who deal with the dependence of the color change of the intraionoic dyes on the polarity of the solvent. According to this conception the dyes ire divided into three types: Some deepen the color with the decrease of the dielectric constant of the solvent (is type), the others increase it on the same congitions (2nd type), and the rest have an intermediate position Card 1/3 (3 r type). The monoanils of clutacone aldehyde as derivatives Alonoanlls of Glutacm 2dehyde. 11. The Influence of .30*f79-28-6-55/63 the Medium on the Color of the Derivatives of Primary Aromatic Annines of the primary aromatic amines are tautomeric compounds the structure of which can be represented by the mentioned formulae of scheme 1. They belong to the intraionoic compounds. Each of the mentioned formulae can be represented in form of a di- polar ion. They easily react on changes of the medium by changing their own color in various "neutral" solvents and in the presence of acids and alkali liquors. However, different from the earlier investigated intraionoic compounds (Refs 6,7) no fixed de;erd- once of the color change on the polarity of the solvent was noticed. Therefore the authors had to inveotiCate this problem more in detail: The relatively good solubility of the monoanils made it possible to determine their absorption spectra in many organic solvents. Thus eight monoanils of glutacone aldehyde were investi6ated this way. It was shown that the absorption change of these monoanilines in various solvents is connected with the structure of the complexes of the monoanil an well as with the solvent an such in the case of an equivalent possibility of conversion. Thus some considerations on the causes of the color change of the monoanils of glutacone aldehyde in various Card 2/3 solyentso in the presence of acids and alkali liquors are mentioned. Mononnile of Glutacmo Aldehyde. II. The Influence of ~;U//79-28-6-55/63 the Medium on the Color of the Derivatives of Primary Aromatic Amines It is shown that there is no principal difference between nolvatochromism and halochromism. There are 4 figuresp 3 table and 13 reforences, 4 of which are Soviet. ASSOCIATION: Khartkovskiy gosud&rstvennyy uniYersitet (Kharlkoy State Uni- versity) SUBMITTED: April 12, 1957 1. Organic compounds--Chemical properties Card 3/3 5 9 9 - 5 - 2 46 OTHORS: Rrigorfyeva, 11. Ye.j Gintse, 1~ K., Af&naq1.,,ea, Z. 1-1. TITLE: Pyridine Dyes, Derivatives of the Secondary Azines (Piridiriovy- ye krasiteli-proizvodnyyP vtorichnykh aninov) -2_7RIODIC.*,L: Zhurnal obshchey khimii, 1059, Vol 29, Nr 5, pp 8617-8619 (USSR) A 3 ST R A CT There are only little data available cr. these dyes (Refs 4,2). As to color and chemical uroperties they are considerably dif- fering from the corresponding derivatives of the primary amines. It can be seen from a comparison of the data pre3ented in table 1 that the unsubstit-ited dye is colored more intensely than the corresponding IN-alkyl-3ubstitnted dyes and that the substitution of the phenyl radicals for the hydrogens of the amino groups is without any effect cri 'he shift of the ab- sorption maximum. The aniline derivat"ie is readily hydrolyzed; the acid suppreoses hydrolysi!j; in ricid solution the extl4nation coefficient increases by more than two times whereas the ab- sorption intensity of the secondary am;ne derivatives is hardly changed by the additicn of acid. It could be concluded from a comparison of the data given in ta~'.~ 1 "hat "he Card 1/3 derivatives of the secondary amnines are not hydrolyzable. Pyridine Dyes, Derivatives of the Secondary Amiries SOV/79-29-3-24/61 Table I illustrates the results of the optical changes of the freshly prepared solutions; on the determination of the variation in the color intensity of the dyes in the tame ccurae, in dependence on the concentration, It can be seen that the derivatives of the secondary amilnes hydrolyze as well, the more rapidly the less the basicity of the cation and thil con- centration of the dye ia. An can further be scon the N-methyl - substituted dye hydrolyzes letat, considerably, however, the diphenylamizin derivative. These facts show that the hydrolysis of derivatives of the secondary arJnes is also related tc the basicity of the cation the degree of wh4 ,ch is determined not only by the nature of the r~~dical b,-It ais~ by itu VOIUMO~ Figures 1 and 2 present the abscrpti~n spectra of the dyes cf the diphenylamine and mothylaniline derivatives In neutral, alkaline and acidified alkaline medium. Figur.-?3 3 and 4 give the spectra of the corres-.1ondini, mcneanils of the glutaconic aldehyde. Four pyri'd-ine dy~','s and twc monoanila of the glutaconic ald,?~~-d,~ werfn synthesized. Fo,.~r preparations are new. It ~o q3ju-e.i thcit the p, oculiar it', ~ 3 -_n. Card 2/3 th(! dyeing of the N-alkyl_sub3tit%t---J dy,~s and their ~.'Lea-;aC- SO 7, '7,2 2 '. Pyridine Dyes, Derivatives of the Seccndary A::;4.re.9 ASSOCIATION: SUBMITTED, Card 7/7~ under the influence of alkali liquor are due to of the spatial arrangement which is inaicated ly their -3orption spectra. There aro '# figureo, 3 tnblos, arnd I? ref- eronce3, 11 of which are Soviet. Khargkovskly gosudarstv,~nn.,-y uziivursA`tt~t (Khar"kc".. 3tat;~ University) January 28, 1956 5(3) AUTHORSs Voynova, V. N. 30V/79-29-5-57/61 and Dukina, L. M. TITLE: Unsymmetrical Pyridine Dyes Olesimiaetrichnyye piridinovyye krasiteli) PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 5, PP 935-940, (UOSR) ABSTRACT: It is known that the color of the unsymmetrical dyes represents in a certain degree a "molecular mixturell of the corresponding symmetrical dyes; the color of thc unsymmetrical dyes has, however, not always an additive character (Ref 1). The authors completed the chemical and spectroscopic investigations reported in references 2-5 and analyzed the absorption spectra of 17 pyridine dyes obtained b;~ them according to Zinke (Ref 6). These dyes were qynthesized by the condensation of the N-substituted monoanils of the glataconic aldehyde with aromatic amines in the areuence of acid according to the well-known scheme 1. In order to avoid the disagreable Card 1/3 intensification of the color of the alcohol solutions of Unsymmetrical Pyridine Dyen SOV179-23-3-37161 the dyes by hydrolysio hydrochloric icid vias added to the alcohol solutions in the spectroscopic investigation of unsymmetrical dyes. Table I gives the data of the optical determinationi of' the. unaymmetrical and the corresponding symmetrical pYridine dyes. The maximu-n values of the symmetric-al does, the 3eccndarj amino derivatives, are presented in column (I), the primari amino derivatives in column III), the calculated Dilt-01). 2y ~i comparison of additive maximum in cola::in 2 the data Civen in triblo 1 It r!iri b4! t;n,,-tj th:st ther colorcil' eight dyiii la of additive nature, that in six dyes (1,4,6,7,11,14) a hypsochromic shift from the additive maximum is observed and that in three dyes (9,15,17) the maximu,:, moves in the direction of the long waves. It is thus seen in most of the CWIC'S that the change in the color depends on the chang .,c of the basicity of the amines which form the molecule of the unsymmetrical Card 2/3 dye (according to Kipri-inov, A. I. nnd Pil~-ugin, G. T-)- Unsymmetrical Pyridine Dyes 3()7/79-29-3-37/61 There are 2 tables and 9 references, 6 of which are Soviet. ASSOCIATIONt Khnrlkovokly gosudarstvennyy univer.,iitet (Khtoekov 3tqte University) SUBMINTED: January 28, 1958 Card 3/3 -.3610 7 -5 9 AUTHORS: Cirigorlyeva, 11. Ye., Glrtoe, 1. K., 1,~,ubit,;kaya, T. A. TITLE Products of lLydrogenlatlon of N-pht--nylpyr1d1n1Lffn Chlorlde. Condensatlon uf N-pheriylpiperldlnium Hydrochloride WIth j)-Dimr--tiiylat-,iltiobeiii-,~ildehy(le PER10DICAL: Zhurnal obstichey Ichlrill, l('60, Vol 30, Nr 3, PP 1031-1037 (USSR) ABSTRACTt This is a continuation of pri~~vious work (11. Ye. Grigorlyeva, A. B. Organeslyan, I. A. My-sh, ZhOKh, 27, 1565, 1957) on hydi,ogen-ation of N-phenylpyridinium chloride (1) over a platinum catalyst under different conditions. The method u3ed wa,-, de.,icrlbed previouily (see above reference). Cozideri:~ation of N-phenyl- piperidinium hydrochloride (II) with p-dimethyl- aminobenzaldehyde (11I) wa.-, aljo studied. It was fovind that an hydrol,,oiiation ol',* (I) over a platinum catalyst, a mixture of N-phenyl- and 11-cycio- hexylpiperidinium hydrochlorldet-, I-, Cormpd. The Card 1/3 Froducts of Hydrogenation of' N-phenylpyridInItim 76305 Chloride sov/79-30-3-59/69 hexylpIperidInfum hydrochlov1de.,3 Is f*or:ried. The ratio of' the two hydrochloride. In the mixture depends on the conditions of' hydi,ogenatIon. Condensation of (II) with (III) in acetic anhydride first form.3 a blue dye. The latter Is unstable and on heating decomposes with formation of a red dye. The blue dye was riot Isolated. It- color Is very close to that of Mlchler-'r, benzhydrol, Etr-,~l 11~, Is t!-,at, they are atialog,.- Thf! ve(l dy#~~. !--~ -ooluble In water, more joluble In and d1chlorcethare. It does not crystallize, and ha.,i the following a~sorp- t1on maxima: In alcohol ll(-'O, III Witel' 501i, and Iri dichloroethane 5011 111 It 1,, ~,,tiggeoted that the re-d dye Is a salt With ti,tictuve 1: Card 2/3 Products of' Hydrogenation of 11-phvnyl- pyridinium Chloride ASSOCIATIONi SUBMITTED: Card 3/3 c11, \N' sov/79-30-3-59/69 b There are 2 figures; 2 tables; and refevences, I U.S., 2 German, 2 Soviet. The U.S. reference Is: C. F. Winans, H. Adkins, J. Am. Cherti. Soc., 511, 306 (1932). Kharkov State University (Kharkovskiy gosudarstvennyy universitet) September 1, 1958 T_4 GIRIGORIYEVA, N.Ye.; KRUGLYAK, L.P.j SHCHERRAKOVA, L.I. Absorption opeotra and structure of glutacona2dehyde dianils. Zhur.ob.khi:-n. 31 no.8:2599-26Q4 Ag 161. (MMA 14:8) 1. Eharlkovskiy goeudaretvennyy universitet. (Glutaconaldehyde) (Amines--Spectra) GRIGORIYEVA N.Ye.- SHCHMIJAKOVAP L.I.; GINTSE, I.K. - 2 --- A Catalytic hydrogenation of di&xLUo of glutaconaldehyde and their o1a to (pyridine dyes)* Ukr.khim.zhur. 28 no.7:848-851 162. (MIRA 15:10) 1. Kharikovskiy gooudarstvennyy univeroitet im. A.M.GorIkogo. (Dyes and dyeing) (Glutaconaldehyde) (Aniline) GRIGORIYEVA, N.Ye.; RODIONOVA, L.A.; S!:GJZWtKOVA, L.I.; Ty7jPA, D.P. Certain transformations of glutaconaldehyde dianils. Zhur. ob.khim. 32 no.2:493-301 F 162. (I-IM 15:2) 1. Kharlkovskiy goeudarotvennyy universitet. (Glutaconaldohydo) S/062 63/000/002/UO4/02'0' B1447BI66 ALITHORSo Mayranovokiyl S. G., Grigor'y-eva-,__t._1m,., Burashkova, H. V., and Kucherov, V. F. TITM Conjugation factors in cyclic eyetems. Communication 6. Polarographio and potentiometrio study of electron interaction offeoto in cyolohexadintio-1,2 dioarboxylio acids and their methyl esters PERIODICALs Akademiya nauk SSSR. Izvestiya. Otdeleniye khimicheskikh nauk, no. 2, 1963, 240 - 245 TEM Cyclohexene and cyolohexadiene-1,2 dicarboxylic acids and their dimethyl eaters were studied polarographically and potent tometrically to clear up the problem of possible interactions between the double bonds of the rIng. The polarograme of 0 CH CO CH CO CH 2 3 2 3 2 3 02 CH OFC02 CH3 C02CH 3 Card 1/3 3/062j63/000/002/004/020 Conjugation factors in... B144/B1a6 CO2CH3 rNFCO 2CH3 0 2CH3 CO2CH3 1',, /ICO2CH3 02 CH3 (IV) (V) (VI) were taken at 250C using 0.05 M tetramethyl ammonium iodide solution con- taining 9.5%, by volume ethanol. The effect of pH and ionic strength was inve3tigated in borate buffer solutions (P11 7 - 10-5), 0-1 N MaOll, and potassium chloride solutions. The anode was an Hg electrode, the reference electrode was a calomel half-oell. The ionization constants were determined at-j200C and init4al concentratione of 1,,0.001 11. For all compounds except III the reduction wave was pfl-independent or I, II, V, V1 the ion trans- ferenco number Is 2, the diffusivity 6.5,;0-9 CM2/sec. The polarographio curves showed two steps; the difference between their B 1/2 could be altered neither by incren8ing the depolarizer concentrstion nor by raining the temperature and ionic strength of the solutionnorby varying the height of the Hg column. This indicates that the two reduction steps are irreversible and occur due to hydrogenation of the double bond involving formation of a relatively stable free radical intermediate. 1%) 1V, the two double bonds Conjugation factore in... B144/3186 are hydrogetiated successively. Electrochemical reduction was-, ababnowts-118W. where the double bond is conjugated with neither of the two GO 2OR 3 groups" All this wan confirmed by the analogoun relation between Ionization con- atanto and utructures of the corresponding acidn. it was found that the eater is more easily reduced and the dissociation constant of tho aci4l increases on conversion of I and V into II and VI respectively. Since the steric interaction of the &tome does not change# these effects must be attributed to Fin electron interaction between the isolated double bonds in 11 and VI. There are 3 figures and I table. ASSOCIATION Inatitut, organicheakoy khimii im. N. D. Zelinskogo kkadsmit nauk SSSR (Institute of organic Chemistry imeni W. D,. tellaskly of the Academy of Sciences USSR) SUBMITTEDt May 10, 1962 Card 3/3 -P, BELOV) 1,, inzh.; GIUGOXI-=A,_O,, Inzh, "Topaz-211 and "Start-211 pocket radios. Radio no.9:38-39 S'63.( RA!6: 1. Institut radioveshchatellnogo priyema i akustiki imeni A.S. Popovas CRIGWYEVIA, (). A.: ~Jartor Mod Sci (dirs) -- "Clinical obseinmtions in acuto hepatitis treated with Intravermi (h-op txansnision of t:..lucosell. Lenint~rfvl, 1")"),10 17 PP (joeningrad rodlatwlc Med Inst), 250 copies (fm, NO r, vr),?, 1,1.1) KIIONHLOV, V.V.; GRIGOR'YEVA, O.A.: RIVLINA, N.Ya. Accuracy of the spectrum determination of the content of a series of elements in metallometric samples. Zap. LGI 39 no.2:149-162 161. (MIRA 15:2) (Ores--Sampling and estimation) GRIGORIY.EVA# O.A.; KVYATXGVSKIY, Ye.M. Ifighly sennitive double-are muthod of spectrograltle antily,11-- for the detection cf gold and some disseminated ele-ments. Zap. LG1 45 no. 2;74-80 163. Okllrul 1-?:5) L nD72-65 WT(M)1XIT(C)1ZWA(d) EWPW/T Pc-h/I`r44/Pv-4/Pi-4 UL/ AM7TF~ASD(&)-5/ESD(dp) RKM jW/JD ACCESSION NR: AT4047300 S/3115/64/000/021/0344/0358 (,6) AUTHOR: -Burovoy, 1. A.; Yemel'yanov, S. V.; Moroiova. K. S.; GrIgorlyeva, 0. A. TITLE: The use of variable structure feedback systems In the controi of thermo- chemical terogeneous processes SOURCE: ~Scow* Gosudarstyenny*y InstItut tsvstny*kh metallov. Sbornlk nouchny*kh trudov, no. 21, 1964. Matematichesklya modell tekhnologicheskikh prot3essov I razrabotka sistem avtomaticheskogo regullrovanIY8 5 peremennoy strukturoy (Mathe- matical models of technological processes and development of variable structure feedback systems). 344-358 TOPIC TAGS: variable parameter control system, automatic regulation, heterogeneous: process, thermochemIcal process. ABSTRACT: The most convenient and effective regimes for thermochemical hetero- geneous processes cannot be controlled by linear methods because the variables which must be controlled are described by nonlinear differential equations with unstable singularitles In the phase plane. The stability of these points depends largely on Initial conditions, so that In order to accommodate realistic distur- bances In the system, feedback controls with variable structure must be used. Using,W method of multi-sheeted phase planes, developed by V. Ve Petrov and Card 11 UO72-65 ACCESSION NR: AT4G47300 G. M..Ulanov, the authors studied the phase plane topology as a function of the sign and magnitude of the static gain coefficient K, of the control system. This Is done by assuming a process with two slngularltla~ only, deriving the expressions for their phase plane coordinates for processes limited by constant velocity of he-t face che-mIcal reaction or concentration of the gaseous component, or by both4,urnd Invastljat_1ngtheba~havlor ~of t-hase ~c-oordI6-aites a-sK. c anges. was ~ discovered that If M crIt;#tboth singularities change pl9cas and lfo~l Kp crit than does I ln?luenc he coordinates very much. This leads t he conclusion %tat I fthe system structure (Y Is varied during the transient pro- cess, the system can be organized in such w3y that It will return to the origtn from any given Initial point and will have a very wide (sometimes unlimited) stabled region. OrIg. art. has: 13 equations and 8 figures, ASSOCIATION: Gosudarstvenny*y Institut tsvetny*kh metallov, Moscow ~$tate SUBMITTED: 00 ENCU 00 NO REF SOV:.11003 OTHERS. 002 Card 2/2 SUB CODE: le'~W GRI VA~ O.D. (Ioningrad) Intravenous drip infusions of glucose in -Boticin's disease. Klin.med. 35 no.8:106-109 Ag 157. (KIRA 10M) 1. Is fakul'tetskoy terapsyticheskoy kliniki (zav. kefedroy - zasluzhennyy dayatell neuk prof. Y.A.Valldmen) leningradskogo Pediatrichaskogo meditsinskogo institute. (HIMITIS, INECTIOUS, ther. glucose, intravenous drip infusions) (GLUCOM. ther. use infect.hepstitim, intravenous drip Infusion) GIIGORIYEVA, O.D.,, kandomed.nauk Dynamics of serum protein fractions in acute hepatitis. vor'. pat. krovi i krovoobr. no.5:69-61 '59. (14I;-.A 15-4) (HUATITIS9 IWMTIOUS) (BLOOD PROTEMS) (PAPER ELECTROPHORMIS) GRIGORIYEVA, O.De, kand.med.nauk Electrophorotic studies of blood protein fractions and hemo- sedimentographic observations in rhe=atic fevore Vopepat* krovi i krovoobore no*6t73-79 t6l. (MIRA 1613 (EfEMTIC nTM) (BU)OD-SEDDMTATION) (EWD PROMNS) 4-~ SMMIOVA, A.M., kand.med.nauk; ~RI O.D., kand.med.nauk Clinic4l serological parallels in rheumatic fevvr. Vop.pat.krovi i kravoobr. no.6:8048 161. (MUU 1613) 1e 1z Fakulltetakoy terapevticheskoy kliniki Leningradokogo pedia- tricheskogo meditsinskogo institute, (zav. - prof. V.A. Valldman) i Otdela mikrobiologii Instituta eksperimentallnoy meditsiny AHN SSSR (zav. - chlon-korrespondent AHN prof. V.I. loffe). (MiEUMATIc nTER) (SEROLOGY) -.T r Rrid f- ft I t 1 ri Ix t I!;, me. 11 to if; ~Aoilc, r- I I t I tJI dE 14 7 .,j- 3 I j j k Grii,'01"Yeva, 0. G., ResiuLance of' coa.,it,o iwint I)y L, n, Tr. Goo. gidrolog. III-ta (WOrIM of' thu Stitte lVdrological. In.;tItute), p 5-28; (MiGeofiz 1/60-M) tl;RlTr!OR'TNA, 0. Ctind GF~q-~r Sei (diss) - - r,,slls'.anc,~ to wavF- acl.!on of shorelinrs composed of coliesive and semtrock stonp". Inin,-rad, lq,~O. 17 pp (Lenin-,rad Ord,-,r of Lenln State U Im A. A. Zlhdanov), 225 cop!es ('~---No 15, 1940~132) GRIGORIYIVA, O.G. Laboratory determination of the resistance of rocks to the action of waves* Trudy OGI no.74:71-88 160. (KIU 13: 7) (Rocim-lestlog) (Beach erosion) GRIGORIYEVA, O.G. Comparing calculated and natural profiles of coastal rhallow!. Trudy GGI no.8809-76 161. (MIRA 15:2) (Coasts) G GOR I General forecast of cbanges in the banks of the Volgograd Remervoir. Trudy GGI no.108:68-88 163. (MIRA 16:6) (Volgograd Roservoir-Shore lines) Ev, C. p r f 1 I of baris TrAy ~."!7-`. 17: 12; SWIRO, I.I.; AMOV, F.G. Prinimali uchastl": PSGUSHEY, M.Te.; GRIGORI j STOYA. POPOTA, L.P.; GONCHAROY, M.Ts.; TOLKI ,T (XIIIA, G.Ye., tokchn.red. (General machinery industry tims norms for establishing norms for milling machine operations; small-lot 3nd piece production] ObahchemashInostroltellur normatIv7 vremeni dlia tekhnichaskogo normirovanlia robot no frezernykh stankakh; malkoserilnoo i edi- nichnoe, proisvodstvo. Moskva. Gos.nauchno-takhn.izd-vo mashino- stroit.lit-ry, 1960. 142 p. (MIRA 14:4) 1. Moscow. ?Sentrallnoye byuro promyshlonny),.h normativov po trudu. 2. 7aveduyushchly otdolom mashinostroyeniya TSentrall- nogo byuro promyshlennykh normativov po t d ri N chno- isoledovatellskom institute truda (for Sh7piuroK nu (Metalwork-Production standards) GRICCRIYEVA 0 P V.G.Shtofkn an a scientint and teacher. Biul.MDlP.Otd.blol. 67 no-5:150 S-0 162. (MM 15:10) (SHTEFKO, VLADIMIR GERM&NOVICH, d.1945) POLUSHRIA, T.V.; RUDIIITSKAYA, Antishock fluid on the basis of plasma albumin in donor blood. Probl.-gemat. iperel. krovi 5 no.3s52-55 Mr 160. (MIRA 14'-5) 1. Iz TSentrallpogo ordena Lenina instituta, gematologii i perelivanlya krovi (dlr. - keystvitelonyy chlen AMN SSSR prof. A.A.Bogdasarov). (SHOOK) (ALBU14INS-THERAPEUTIC USE) 1. GRIGOR1M'.,',, O.V. and KFLIZON, 1,.S. "The Dynamics of Proportional Navigation." Notes of the Leningrad Higher Engineering Naval Academy im. ndmiral S.O. Wnkarov, Issue 1957- -,.;. ,.') . 11, LUTHORt A.S. and Grigorlyeva,O.V. SOV/20-121-3-10/47 Kel'zon , (Leningrad) TITLEs The Proportional Wavigation as a Problem of Cybernetics (Proportsionallnaya navigatsiya kak problema kibernetiki) PERIODICALs Doklady Akademii nauk SSSR,1958,vol 121,Nr 3,pp 432-435(USSR) ABSTRACTs Starting from the papers of Fewell LRef 1) and Spitz LRef 2] who investigated the kinematics of guided missiles, the authors consider the dynamics of guided missiles under proportional navigation and the suitable choice of a control of motion which would guarantee a stable tending of the object to the target. The consideration of the dynamic equations for the considered motion admits to explain partially the apparent discre anciea (the necessity of non-hitting) in the papers of Looks fRef 61 and Adler [Ref 91 . There are 10 references- 3 of whioh are Soviet, and 7 American. ASSOCIATIONs Leningradskoye vyssheye inzhenernoye morskoye uchilishche imeni admirala ?TnkArova (Leningral HiOier School of lqaval En'l-intering imani Admiral Mlkurcv) PRESENTEDs 'Y"arch 27, 1958, by V.I. Smirnov, Academician Card 1/2 4a 0 AUT:4URS G r i & 0 r I Y cYAq- U. V. , TITLE: The calculation of guidance problems FENIODICAL: Jzvestiy~j vys.-illij,11 Aviatsionnaya tekirlika, ~:/147/61/OOU/004/003/021 E031/E184 and Ke Vzon, ,,. S. control inert ja it, c(.~rtaijl jjcjjebljyj~LI I V., '6-t, (It, tj I-y no.' , 11)61, 2~-'-"q "' I -:XT It has been shown that all est ivjttezi (if manoeuvrability based on the value of the normal acceleration of the centre of inertia are inadequate. The conditions of stable missile guidance with consideration of the inertia of the controllini; airfoil are discustied for tht,, following ca!3es of .1) with a zero lead angle (pitro purtiuit cotirqe); 2) %,rith a constant lead angle (deviated pursiiit course); and 3) with the'use of the proportional navigation course (approach). The limit values, in pursuit courses, of the velocity and acceleration of the control-flap declination in the filial stage of approach are determined from given formulae for certain values of It = vs/v (vs speed of the target, v = speed of missile inertia centre). In the proportional navigation course Card Th(_. :,Itions of control inertia. fi/l"17/61/ooo/ot)"i/oo-71/021 *EO31/El8,,i equatAon '~ of motion are given for the navigat ior,a I I-t ion A = 2 ; L h o ~-, o 111 t io 11 shot"_', tild, -c la t. I olis I I I p 1, " i .. i, , ~1~ ~i rl~~ Ie of contro 1-f 11,% 1) tl(~c 1. irwit ion and t if(,- lead 1 4~ . T~,, I , rt~ 1 -! t I onfilli p ensures that toi- controlled object will t'o I 1mv. the ti "jectury exa c t ly. The Condition for hitting the t.tr~,:et is 1) >1 (p=1/1,;). The stability boundaries for guidance of the mi.-;54f Ie ill the firlal St;AS(' 11-e Ca ICU lated from the turnin,~ rate of the pa t. h while velocity and acceleration are determined from thQ control- fla,) declination. The results are plotted in a dlagrat:i f rom which the effect of the control-f tap inert la can be determined. $ ince thf~ pursu j t courseLq are part j cu I ar ca.5e.,5 of the. proport iona I navi.c_iAtion course with A = I , it is conclujed t~j;it. the increatie of t!1(! llovigatiollill Correction widells the I it y the -uidalice of a Inissile in Lhe final tit' its There are 1. figure and 2 tables. ASSOCIATION: Kafedra teoreticheskoy mek-hArliki, d!ikove vy!3slieye inzileneriloye morskuy., och i, I 1~-,hchv (Department of Theoretical J,on~ngvad C,~trd 2/21 Naval Enginnering 1'1~gh School) S 1: BY I TT E D january 23, 1961 GRIGORI)~".V.; KELIZON,, A.S. Considering the inertia of the rudder in some problems of pinpointing, Izvvyo.uchebozav.; av.tekh. 4 no.4:22-29 161. (HIM 15t2) 1. Ioeningradskoys vyssheye inzhenernoye morskoye uchilishche. kafedra teoreticheakoy mekhaniki. (Bombing', Aerial) FEDOROVA, L.I.; GRIGORIYEVA, O.V.1 KOZINETS, G.I. Preparation of plasma by formation of Increased pressure in flasks. Probl. gemat. i perel. krovi 9 no.3t57-58 Mr 164. (MIRA 17s10) 1. TSentralInyy ordena IAnina institut gematologii i perelivaniya krovi (dir.- dotsent A.Ye. Kinelev) Ministerstva Mravookhranenlya SSSR. GRIGORITIVA, P.Y4.4jots. A.F. Koni and his work in the field of Passian forensic medicine, Trudy LNI 2.,295-300 155 (Nnu 11:8) 1. Kafedra, sudobnoy meditsiny (sav. - prof. A.P. Kurdymov) Pervogo Laningradskogo seditsinskogo Institute ImenI akadealka I.P. Pavlove, (MVI. ANATOLII FREDCROVICH. 194-4-1927) (MICAL MISPRUDOGS) DONIGISVICH, M.1.9 kand,med.nauk; GRIGORITIVA, R.I., kand.med.nauk; ZHUCHKOVA, L.O.; XADOWSMVA. P.P.; SiMINOVA, X.P, (Nor-dovskaya ASSH) Organization of psychoprophylactic preparations for all p&rturients in Saransk. Top.okh.mat. I dot. 4 no-5:74-78 S-0 '59. (SAW SK--CHIUM MrH-PSTCHOWOT) (KIRA 13:1) SOV/110-59-6-3/24 AUTHORs Sakovich, A.A., Candidate of Technical Sciences; Grigorlyeval Rol., Engineer; Grigorlyev, V.S., Engineer and Blonds I*Vol Engineer TITLEs An Investigation of a Titanium Absorption Pump (lealedovaniya titanovogo absorbtsionnogo nasona) PERIODICAL:Ventnik elektropronyahlonnosti, 1959, Nr 6, pp 13-16 (USSR) ABSTRACT: Existing types of vacuum pump are subject to various operating difficulties when installed on high-voltage valves. The pump here described is based on the principle that titanium does not react with mercury but can absorb gas when hot. Hot titanium reacts irreversibly with most gazes and volatile organic compounds. Theme substances penetrate the crystal lattice of the t1taniums forming solid solutions. Zxcept for hydrogen, gases thus absorbed are not released during subsequent heat-treatment under vacuum. This principle formed the basis of the model absorption pump which is illustrated diagrammatically in Fig 1. The absorber in a block of porous titanium containing a heater. Because different parts of the block are heated to different Card 1/5 temperatures different gases are absorbed. The device SOV/110-59-6-3/24 An Investigation of a Titanium Absorption Pump was found to be fairly effective at pressures between 0.5 and 0.001 mm Hg. As porous titanium contains a considerable quantity of occluded gas, prolonged de-gasification was necessary. The device does not absorb inert gases and evolution of hydrogen is possible if the thermal conditions are unsuitable. Titanium absorbs gases beat when it in condensing on a surface and attempts have been made to use this principle in the construction of pumps. However, as pumps of this kind are complicated and unreliable, improved methods of atomising titanium were sought. It was accordingly decided to locate the titanium in the mercury cathode and atomise it by ionic bombardment in the presence of a cathode spot. A model absorption pump constructed on this principle is shown in Fig 2i it in installed in a high-voltage valve. Authors' certificate Nr 111517 of Ilth March 1957 has been taken out by three of the above authors for this device. The titanium electrode in on the centre line of the valve and is surrounded by an Card 2/5 auxiliary electrode at a positive potential. When An Investigation of a Titanium Absorption Pump SOV/110-59-6-3/24 negative potential is applied to the titanium electrode an ionic current passes causing atomisation. The atomised titanium in deposited on a screen and on the auxiliary electrode, creating an active surface that effectively absorbs the gas. The screen protects the internal parts of the valve from contamination with atomised titanium. Some results of tests on the absorbing power of atomised titanium obtained with this model are plotted in Fig 3. It was found that when pumping air the lower limit of pressure is below 2 x 1o-5 mm Hg. The weight of absorption with a current of 2.5 mA and a voltage of 2~5 kV for various gases is tabulated; the figures relate to a volume of 20 litres with an initial pressure between 60 and 70 microns Hg. The electrical circuit shown diagrammatically in Fig 4 may be used to supply the electrodes of the device. Employing this simple circuit, it was possible to make up a sample titanium absorption pump and instal it in a mercury rectifier type VR-3M as illustrated Card 3/5 diagrammatically in Fig 5. The valve was subjected to An Investigation of a Titanium Absorption Pump SOV/110-59-6-3/24 -the usual manufacturing cycle of vacuum treatment and forming. After evacuation by a mercury pump, the valve was connected to the absorption pump, Tests were then made on the rectifier on a low-voltage bench and at high voltage using an equivalent circuit. The electric strength was checked periodically by static tests. The valve was maintained for 2000 hours without the mercury pump in use and operated under load for about 400 hours; there was no came of pump failures When the valve was left for a long time without pumping, leakage caused the internal pressure to rise to some 5 or 10 microns Hg but when the absorption pump was connected the vacuum was soon restored. A defect of the pump is that it absorbs inert gases only very slightlyg hence, if there is an appreciable ingress of air, atmospheric argon may accumulate in the valve. The service life of the absorption pump, though not yet established, is likely to be considerable and can probably be made of the order Card 4/5 of 10000 hours. The power required for the pump is about An Investigation of a Titanium Absorption Pump sov/ilo-59-6-3/24 100 W, most of which is absorbed by the auxiliary electrode. By a slight change in construction the latter could be used as an excitation anode; the power required to operate the pump would then be considerably reduced. One of the advantages of the pump is its high pumping speed at low pressures. A disadvantage in the presence of a high voltage on the auxiliary electrode which, amonst other things, limits the upper pressure to between 200 and 500 microns Hg: beyond this limit corona occurs and atomisation of the electrode is much reduced. There are 5 figures, I table and 3 references, I of which is Soviet, I English and I German. Card 5/5 liv.)TOMOV. V.K.; ~OLGV. V.b. Relation between the structure of orpnin compounds nnd their odor. lienort N,7.4: Synthesis of 3-(41-tort-butyl phoivl)-2- T-ady VNIISNDV nn.!?:19-'1')1 1514. 0 -,iA V':7) groixD) (Proplonaldehyde) I- ---- GRIGOR'731VAO S. . , -- -, : -1 . Fr~tt growers frm the Urals. Worov's 2 no.9:26 s '56. (min 9:io) (URAL NOUICAIN PJIGION--"UXT CULTURI) GRIGORIYEVA, S. Vacuum cleaner In the service of science. Zzian.eila 35 n0.1! 6-7 Ja 160. OGRA 13:5) (Seed industry) SAMARINA, V.S.; NOVOZHILOVA, Ye.V.; GRIGORIYEVA, S.A. Formation of the salt composition of underground water in some regions of Central Asia. Vest. IZU 17 no.12:22-31 '62. (MIRA 15s7) (Soviet Central Asia-Water, Underground-Composition) KUZNZTSOV. I.P.; FOIAK. A.Y.; RRIC~~ITNTA, M. Rapid construction of petroleum refineries In Bashkivia. Prom.strole 38 no.6:28-29 160. (m," 13 -, 7) I* Inatitut B"hN113troy (for Grigorlyaws). (Ushkiria-4fttrolaux refineries) GRIGORIYEVA, S.I., inzh.; FEDORTSEV, I.V., Inzh. lArge.-block assembly of tubestills. Trudy BashNIIStroi no.1- 109-121 162. (KIRA 17:3) ANTONOV, A.S.; LAYKOVA, N.F.; IVANOVA, P.V.; GRIGORIYEVA, S.P.; BELDZERSKIYP A.N., akademlk Changes in the amino acid composition of fibroin of the silkworm Bombyx mori L. induced by the analogs of the nitrogen bases of DNA and RNA. Dokl. AN SSSR 155 no. 5:1201-1204 AP 164. (MIRA 17:5) 1. Mookovskiy gosudarstvennrj univer3itet im. H.V.Lomononova. 7 BELOUSOV, M.S.; POKLADA, I.I., prof.; BEZRUKIKII, P.S.; BARNGCLITS, S.B.; ZLOBINA, P.P.; GRIGORIYEVA S T - MEDVEDEVA, R., !%A~! P red.; TELEGINA, T., tekhn. red. [A course in accounting] Kura bukhalterskogo ucheta. 2., perer. i dop. izd. Moskva, Gosfinizdat, 1961. 488 p. (MIRA 16:11) (Accounting) KOVAIMIO. N.I.; GRIGOIRITIVA, T.A. 1 - . , -, Optical activity, density, and molecular weight of oil fractions of petroleum from the Saratoy field, Report No-5- Uch.zap. Sar.un. Typ. fiz. 56:129-138 '57. (MIRA 12:11) (S&ratov region-Petroleum) -TffA13TrEVrZ.S., HUKlNA,Ye.A.,KIHB, M. & dilGall Y-,,'J A . A. --"Fagin-Complex 1"paration for tlw Treatment of Refractorf Infected ~lounds." SOi Byuls Skaper.Biol* i Mede 1944(g),(Quoted in Referaty 19h5) GRIGORIEVA, T.A. "Innervation Of The Internal Organs." (P.134) by T.A. Grigorieva (Moscow) SO: Progress of Uontemporary Biolo (Usp. Sovrem. Biol.) Vol. DIVIII, lc,49, No. 1 (4) (Jifly-Aug.) - -- q~, i~~ _q, I -- - - I - GRIGOR I TEVA, T. A. 29879 ImWervatslya kapillyarov. doklady akad. nauk SSSR. novaya oyeriya,, t. LXVIII, No. 3" 1949, a 589-92. - Bibliogri 11 aasv. SO: L S T 0 P I S I NO. 40 GRIGORIYEVA, T. A. Synapse in region of the capillary bed., Uch. zap. Vt. mosk. med inst. 2, 1951 Capillaries, USSR (600) GRIGORIYEVA, T.A. Cause of trophic disorders in regions of the body deprived of sensitivity. Doklady Akad. naiik SSSR 78 no.2:387-390 11 May 1951.. (CIML 20:9) 1. Second Moscow State Medical Institute Imeni I.V. Stalin. 2. Presentod by Academician A.D. S.peranokiy 26 February 1951. of t,~.(. Sin 1~2, 'cron, "orcov --at(, ~.e~-ucnj ir;~t n. (Dis-ertnti-on for th,~! i)c,lrcp, of Doctorate in lechrrnnya J,=ar-y-Deccmbcr llfl~2 CRIGOROYIYA, Tatlyana Andreyevna; SHUBIN, A.S., redaktor; SACHITA# A-I-# u kyl A rc-li ;-00 F-24,r [Innervation of the blood vessels) Innervatmila krovenoonykh mosudov. Noekva, Go@* Isd-vo, mode Ilt-ry, 1934. 373 P. (MLRA St3) (Blood ves"Im-lumervation) DOIDO-SOBUROV, B.A., professor. radaktor; GIBBILISKIT, N.L., redaktor; redaktor; YILISEYIIV, T.G., redaktor; ZHDAKOT. D.A., redaktor; KNOPPI, A.G.. redaktor KUPRITANOV, V.V., radektor-, NIKHAYWV, T.P.. redaktor; PRIVNSA, N.G., redalctor; STUDIT$Kff. A.S.. redaktor; SHCHILKUNOVA, S.I., redaktor-, KHARASH, G.A., tekhnichs- okty redaktor [Problems in the morphology of the nervous system) Probleny morfologii nemol alatear [Leningrad] Goo. izd-vo mad. lit-rr. Imningradskos otd-nie. 1956e 179 ps (MIRA 10:2) Io Chlen-korrespondent Akedemii maditainskikh nauk SSSR (for Dolgo-Soburoy) (UnTOUS SYSTM) USSE/General Division. History. Classics. Personnel. A-2 Abs Jour., Ref . Zhur. Blologiia,, No 4, 1956, 14131. Author Grigorev&_Z.A. Inst Title I.M. Sechenoy and His Thoughts on the Structure of the Nervous System (On the Fiftieth Anniversary of His Death) Orig Pub: Arkhiv anatcaii, gistol. i embriologii, 1956, 33, No 2, 7-13 Abstract: The numerous hypotheses of Sechenoy on the structure of the nervous system, which were confirmed bylster research, are cited. The under-estimation of Secbenov's hypothesis tbat the inhibiting fibers are intercentral and end, not in the skscles, but in the corresponding nerve centers, is pointed out. Considerations an cited again t the newest propositions on the interchangeability of nerve elements. Card 1/1 -7- GRIGM17EVA. T.A.; LUVICH, G.A. (Moskva) Meeting of the Moscow Society of Anatomists, Hiotologists, and Imbryologletso Arkh.anat.glstol enbr. 33 no-3:10D-101 Jl-S '56. (MIRA 12-.11) (AWATONT--PMODIC&W) . A- (Moskyap 1-41, 1-ya Neshahanskaya. d. 90/96 90 The structure of unnWelinated nerve fibers; review of foreign literature. Arkh. anat. gist. i embr. 34 no.1:121-128 Ja-F '57 (KLRA 10:5) 1. Ix kafedry gistologii (zav.-chl.-korr. AN SSSR. zaal. deyat. naukil prof. G.K. Khrushchov) I! Mookovskogo gosudaretvennogo meditainakogo instituta im. I.T. Stalina. (NIMUS, anat. and histol. unmyelinated fibers structure. review) XJJORIJ;TA-.Z.A. (Moskvn, 1-41. 1-ya MeahchnnekAya ul.. d.gn/96, ~v.q) ",toixrnn1 of comparative neurology" 1956. Reviewed by T.A.Grigorleva. no.6:118-124 fi-D '57. (N-,UROLOGY--MU IODICALS) Lin Nngllohj, Vols.lo4-lo5. Akrh.nnnt.gist. i embr. 34 (MIRA 11:1) GKIGO;QmA-j-TvA.-, prof., red.; ZEIZNINO A.V.p kand, med. naui,.# red.; SAVICH, G.A.9 1-cand. mod. nauk, red. lftommtions of the First Conference of Young staff Members of Morphological LaboratorieB in Moscow] Trudy pervoy konforentsii molodykh nauchnykh sotrudnikov maskovskikh morfologicheakikh laboratorii. Pod red. T.A.Grigorlevoi, A.V.Zelenina i G.A.Savich. Moskva, Vses. ob-vo aratomovp gistologov i embriologov, 1959. 139 P. OAIRA 15:4) 1. Nonferentaiya molodykh nauchrWkh sotrudnikov moskovskikh mor- fologicheskikh laboratorJy. lot. (14orp~ology(An:Lmals))-Congresses)) GRIGORITIU, T.A.t prof, Kwous w"r no. Zdorovlo 6 se.6t9-10 Jo 160. (MIRA 130) (Nmms xNalin) GRIGORIYBVA, T.G.-.- Results of testing baits to control agr1otes obscaras L. Trudjr VIZR no.1:157-160 148. (MIRA 11:7) (Click beetles) (Insect baits and ropollents) I ~fl so dkma go's it A I al L L"IMUNI CLAIWKATNP 2#1401 *to diff set AV so Is 1, -6 a 0*0 0* 00099 0000000 I-Off a ~11 1w 0 u At a of w a a --a-- Ito$ #00 0660#81646 w0fe coo gee see elf I-so 141914ftf O"'Ai W 94. " i I ?A &s& is 00900*000000*00410 0 a a1 , A ussR/Diology - Rexachlorane as an Insec- Dec 52 ticide "The Effect of Hexachlorane Deposited in the Ground, on the Fauna of the Soil," T. G. Grigoryeva. (Submitted by the Section of Plant's Protection, All Union Acad of Agric Sci. imeni V. I. Lenin) Dok V-S ord Lenina Akad selkhoz nauk imeni V. I. Lenina, No 12, pp, 16-20. Describes the toxic effects of Hexachlorane on the insect fauna of the soil in selected exptl sections of the Leningrad Oblast. Observations over a period of 3 years, revealed the potency of hexachlorar-e in dwtvvylft haorul plant-40tUo inseci-g-aa- FrQfttWI*S 1u =d SbOwO ground, Vith little or .no orfact on rain ww , and. sow beneficial er- feet on certain plants, resulting in increased Croper of agricultural plants grovn on soil treated with hexachlorame. 248T2 GRIGORIYIVA. T.0.; XARMVA, A.I. 7eeding specialization of the frit fly Oscinella pusilla Haig. in the trans- Volga region. 9001-9hur. 32 no.5:893-902 5-0 153. (HLRA 6:10) 1. Veanoyuxnyy nauchno-iselodovateliskiy institut sashchity rastenly. (Volga valley--Yrit flies) (Frit flies--Volga valley) STIRK. V.S.; GRIGORIYEVA, T.G. In mmory of Georgil gonstantinovich Fistnitskil (1900-1931). Ant.obos. 33:376-379 153. MIA 7:5) (Piatnitakil, Georgil Konstantinovich, 1900-1951) GRIG OR I I-ATA. Tat 'yam Grigor lyevuu. [~~O-C~two*rm Haden& baellIfnes and its control] Zervcyvye sovki i bor%a a niml. Moskrap Goo. izd-vo sellcoz. lit-ry, 1958. 56 p. (Grai&-Diseasos and posts) (Outworms) (MIRA 11:10) GRIGOR;rEV -' starshly nauchnyy sotrudalki GLEBOV, M.A., startihiy A I ,,, nauchnyy notrudnik; FERSIN, S.A., starshiy nauchnyy Botrudnik; FETRUKHAP 0'1., otarshiy nauohnyy sotrudnik; SLIVA, I.K. Practices in effective control of the sugar beet weevil. Zashch. rast. ot vred. I bol. 4 no.5:23-25 S~-O 159. (MIRA 16:1) 1. Vsesoyuznyy institut sashchity rasteniy (for Grigorlyeva, 'Uhbov, Persin). 2. Vsesoyuznyy nauchno-issledovatellskiy Inatitut sakharnoy svekly (for Petrukha). 3. Glavnyy agronom inspekisil po sel'skomu khozyayotvu Smelyanskogo rayonei, Cherknaskoy, oblasti (for Sliva). (Smela District--Sugar beets--Diseases and pests) (Smela District-Weevils--Extermination) GRIGORIYEVA) T.G.,-k&M.ael'skokhoz.nauk Imediate tasks in the protection of grain crops. Zashch. rest, ot vred. i bol. 5 no.9:1-3 S 160. (MIRA 15:6) 1. Zaveduyuohohiy 3,aboratoriyey po izucheniyu vrediteley zernovykh kulltur Vaesoyuznogo instituta zashchity rastoniy. (Kazakbotan-Wheat-Disoases and posts) oRXoR, iTvA , 2. ra. ---- ---.---Nw-~-9e,nera1 law governing the formation of agroblocoenosem and principles underlying the protection of plants on virgin lands. Zhur. ob.'Ibiol. 23. no.6:411-418 N-D 160o (KIFA 14: 1) 1, Vessoyusnyy nauohno-iseledovatellskiy institut sashohity rasteniyq Leninarad. (RECLUMION OF LAND) (AGRICULTMULL PESTS) GkIGOR'YXVA, T.G. Factors determining methods used to protect grain crops in the region$ of reclaimed virgin and Idle lands. Aht. oboz. 39 no-3:509-520 160. (MIRA 13:9) 1. Vnesoyuzwy institut sashchity rasteniy Veemo7uznoy akademii sel'skokhozyaqstvannyykh nauk 1m. Lenina. (Kazakhetau-Wheat-Diseases and pests) GRIGORIYEVA, T.G.; TERSKHRI, E.S. Diatribution of grain hugs of the genus Aelia, (Homiptera, Pentato- 0 midae) in the trans-Volga region and northern Kazakhstan. Ent. oboz. 40 no.la19-23 061. (MIRA 14:2) 1. Vsesoyuznyy institut zashchity rasteniy Vaesoyuznoy akademii sel'skokhozyaystvennykh nauk imani Lenina., Leningradr. (Starays-Poltavka Distriot--4tinkbugs) (Karabalykokiy District--Stinkbugs) (11mat-DiBeases and posts) -GRIGOR3?~~LAI T-G. Some results of azxl prospects for studying the grain Fksts and their control in areas where virGin land is beinf; brought under '1-1-zhur. 41 no.10-17 Ja 162. 04IRA 15:4) lo All-Union Institute of Plant Protection, Leningrad. (Virgin Territory~--Wheat-Diseases and pests) GRIGORITEVI, T.G. Investigation of the soil fauna in virgin and cultivated lands of the trans-Volga region. Vop. skol. 7t4o-41 162. (MIRA 160) 1. Vmooyusnyy institut sashchity rasteniy, Leningrad. (Volga Valley-Soil fauna) T'! GRIGORI)EVAO T.G. Raw crop farming and the main objectives of agricultural entomology& Ent. obozr. 41 no.3:485-491 162. (MIRA 15:10) 1. Veesoyunzyy institut zashchity ratieniy Leningrad. (Insects, Injurious and beneficiall