SCIENTIFIC ABSTRACT OLDEKOP, Y.A. - OLEARCZYK, J.
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S
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100
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December 31, 1967
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SCIENTIFIC ABSTRACT
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77(~041
SOV/79-30-2-5 V
AUTHORS: Olldekop, Yu. A., Mayer, N. A.
TITLE: Decarboxylation of Me.-curic Propiohate With Peroxides
PERIODICAL: Zhurnal obshchey khimii, 1960, Vol 30, Nr 2, pp 619-
623 (USSR)
ABSTRACT: The decarboxylation of mercuric propionate and
acetate on UV irradiation and the decarboxylatiun
of mercuric acetate with various peroxides were
reported previously by the authors (this J., lq6O,
our abstracts 77400; 77404; 77405). The present
study investigates the mechanism of the decarboxy-lation
of mercuric proplonate in reaction with propionyl
peroxide, benzoyl peroxide, and hydrogen peroxide.
Mercuric propionate and propionyl peroxide (in 1-2,,
molar ratio) In proplonic acid were heated at C
for 3.5 hr. After distillation of ethyl propioi-,,ate and
propionic acid, the residue was dissolved in water and
Card 1/7 treated with KC1 to give ethylmercury chloride in 6!.D-%
Decarboxjlation of Mercuric Fropionate With 7790L'
Peroxides SO V/7 'G - 3 0 - 2 - 55,
yield. The mother liquor treated with KI exceos gave
ethylmercury iodide in 27.3% yield; the total yield
of C2H5HgX compounds was 88.8%. The reaction gases
contained C02., Co. CA, C4HIO, and traces of C2Hjj-
The same reagent3 as above, but in a 1:1 molar ra-tic,
gave ethy-Imercury compounds in 65% yield, mercurous
propionate in 18.2% yie.ld, and 13.4% unreacted start-fn-;:
mercuric propionate. Mercuric propionate and benzoy,
peroxide (-in a molar ratAo 3:1) in proptonic acid,
heated for 4 hr at 97-018'j C. On filterin6, 20.1%
mercurous propionate was separated; the filtrate,
after distillation of the solvent, dissolution ci' the
residue In ether, extraction with water, and treaz~in.-
the water eztract with KI, gave ethylmercury iodide
in 54,2% yield. The solvent was evaporated from the
ether solution, the residue mixed with KC1, and steam
passed through the mixture. The reaction gave phenyl-
Card 2A mercury chloride in 16% yield (24% based on benzoyl
'Y
11
Decarboxylation of Mercuric Froplonatle With 7790"
Peroxides SOV,/79-30-2-j5/78
peroxide), and also a small amount of n!-dinitrobenzene.
The reaction gazes composition was qualitatively
identical w1th that Of 't"he
propioi,a~'-Iz,, ~wlth benzoyl pero~tlde (In molar 1'atlo 3:1)
in benzene on heatin.--. at 80() C for 8 kir -ave on
zi,mllar treatzj,,ent IC4 Mel'CUMUO Tj1'OpIO11,'1tt'j' -1 ~b
Phenyl-mercti*ry ('11101'Ide ((5% ba:;ed on benzoylP
14-35% etnyimercury oilorlde, 24.4% ethy1nercury
Iodide, and a zinall amc)ullt of benzoic acid. Con-
:3iderlni; t'alt-, oljtnalned. the decarbo:~ylati(.;11
nechanl:;M of proplonate can be explained by
re -act iono D(10) -
Card 3/7
Decarboxylation of Me-~curic Proplonate With 779,04
PeroxideD SOV/79-30-2-55/78
fRC02~1 211C03 -; 11C02 - 11 - + C03 M
III - CO). C,11.)
C2133COMISOCOC~113 + 11 -%' It J190COC~111 + C-2735CO2 (2)
C211"CO2 - --* C31)7,. + C03 (3)
C21J.-JISIOCO 113 +
1011A + calj:~CO, -~ PAOFA GATI ON
xf,comt,
-3 '
D3- -IVAP~
I
C
C,.,lJCOOC,)JF 4-
2. llgOCO('2115 (G)
Card 4/7
Decarboxylation of Mercuric Proplonate With 77 ~Oi
Yeroxidez 10
+ ]1IF)(OE;O(]0UJ - CI)131190COC,2113 + - 1190COC2113 (7)
C2)13 - + C211g + 11' . M
CMID O'HEItIlime")
The steam distillate, after filtration and separation
of b1phenyl, gave 1.21% ethylmercuryiodIde. Total
yield of ethylnercury iodide was 55.41%. A convenient
synthesis of ethylmercury salts is the reaction of'
mercuric propionate with 42% hydrogen peroxide tit a
mixture of' propionic acid and proplonic annydride. un
heating at 97-9 I'or 2 hr, the reaction gave ',!.36%
metallic 119, 797-elthylmercury chlorldeand 6.354
ethylrnercury iodide (uee method Used in the decal'I)OxYla-
Card 5/'j- tion of' mercuric propionate with Proplonyl peroxide in
Decarboxylation of Mercuric Proplonate With 77904
Peroxides SOV/79-30-2-55/78
propionic acid). Total yield of ethylmercury salt3
was 76.35%. The reaction gave also mercurous
c>
ProPionate in 1.95% Yield, and 16.6% unreacted
Btarting salt. The presence of dimethylsuccinic
acid waz detected, and its formation can be ex-
plained by reactiono (11) and (12)
q111 + u.1ducooll , III)
C113C)IC0011
2en'tilcooll _-1.I (n)
C11,C)IC0011
There are 10 references, 2 U.S., I U.K., 1 Ditch,
2 German, 4 Soviet. The U.S. and U.K. references
are: F. E. Blacet, W. E. Bell, Discus. Farad. Soc.,
14, 70 (1953); J. 11. Pitts, Jr., R. S. Tolber6
F. W. Martin, J. Am. Chem. Soc., 76, 28113 (1954);
C. D. Wagner, R. 11. Smith, E. D. Peters, Ind. Eng.
Ch., Anal Ed., 19., 976 (1947).
ASSOC;A ION: Institute of Physical Organic Chemistry, Academy of'
Card 0.
Decarboxylation of Mercuric Propionate With 77904
Peroxides SOV/79-30-2-55/78
SUBMITTED:
Sciences, Belorussian SSR (Institut fiziko-organ'Leheskoy
khimii Akadenii nauk Belorusskoy SSR)
February 9, 1959
Card 7/7
DLIIUQP, Tu.A.; AZANUVMLKYA, X. M.
Reactlow of ditertlary butyl peroxide witb mercurous and
mercuric acetates, witb mercuric benzoatB, and witb metallic
mercurys Zhuro'bkbiza 30 no-7:2291-2294 Jj 160.
(MIU 13:7)
1. Inatitut fisikD-organicbOBkoy khizii Akadamii nauk
BolDruszkoy SSR.
Dutyl 3)aroxide) (Mercury) Olercux7 acatate)
CBenzolv acid)
OLIMIXOP, Tu.A.; 1DXL$Ch1X, Z.B.
Photochemical reactions of vercur7 orgatomotallic compounds In
solutions. ]'art 15: Photochemical reactions of mercury-bis-n-
benZDiC acid and Its dimetbyl aster. Zhur.ob.khim- 30 n0-8:
2564-2567 Ag 360. (MIRA 13:8)
1. Institut fiziko-organichaBkoy khlmii Xyzademii mauk Belorutkoy
SSR.
(Ben2Dic acid) tMercunr or&%nic compounds)
OLIJ)ZXOP, Yu,A.; HAYYJM, N.A.; GMnJ2M, Y.1,
Photochemical reaction of n-marcury butyrats. Zhurob.khim- 30
mo.8:2567-2569 Ag ,6o. OaRk 13: 6)
1, Institut fisikD-orgamichuBkoy khImil Akademii mauk -%lorusskoy
SSR.
oatyric acia)
e_: OLIDMP,- Tu.A.; YAYTM- , B.A.
ReactiomB of m-renuTlt caprate with perDxldes. Zhux. ob. kbiu.
30 MD.9:3017-3019 5 360- (MIRA 13:9)
1. Inatitut fizi7rc-organicheskoy khimil Akademil mauk BeloruBskoy
sm
(ParmideD) (Capric acid)
AUVIO-L YU.A.) KALININA A.M.
Reactiona ~of carbon tetrachloride vith benzene homologueo. 22rir.
ob,khim. 30 no.IOJ358-~3361 0 J61. Oa:-A 14 2-4)
I* BelorusAI7 gosudarstw=W iud-veroitet,
(Carbon tetraebloride) (IXOwtic compounds)
- OL..IDZ'KOP~_j-l";4M=- , N.A.
Reactions of mercury chloroacatate and benzoate with peroxidvao
zhw.ob,lc'ni-- 30 =4 :31*72-3476 0 161. (XPA 14:4)
2. Institut fiziko-organicheBkoy khi-mii Akademii nauk BelorusBkoy
SS.R. (Acetic acid) (Benzoic acid) (Peroxides)
88478
~'.PDb
S/079/61/031/001/010/025
B0,01/3-066
AUTEORS: 011dokop, ~u_ Azanovskayat M, M., and Kharitonovich, A. 11.
TITLE: Reactions of Silicon Peroxides With Some Tertiary Alcohols
PERIODICAL: Zhurnal obshchey khimii, 1961, Vol. 31, Wo. 1, pp. 126 - 128
TEXT: Among the numerous reports published in recent years on organo-
elemental peroxides EI-0-0-C and BI-0-0-El (El - Si, B, P, or a heavy
tetra- or bivalent metal) (Rof. 8) also their reaction with tertiary al-
cohols in the presence of acid is described. The authors applied this
reaction also to the synthesis of asycoetric organic peroxides of the
ROORI type. For this purpose they studied the reactions of triphenyl
carbinol with tetra- (teTt-butylperoxy)-silane, trimethyl-(cL-cumylperoxy)-
Bilane, and trizathyl-(diphenyl-mathylperoxy)-silane, as well as the reac-
tions of dimethyl-phenyl carbinol, trimethyl carbinol, and 1-methyl-cyclo-
hexanol -with tetra-(tert-butylperoxy)-silana. Reaction was carried out by
interaction between the tertiary alcohol dissolved in acetic acid (in the
presence of a little sulfuric acid) and silicon peroxide dissolved in ether.
The reaction of triphenyl carbinol with silicon peroxides gave the
Card 1/3
S801
Reactions of Silicon Peroxides With Some S/07~/61/031/001/010/025
Tertiary Alcohols BOO1/BO66
corresponding asymmetric peroxides of the BOOR' type: the peroxides of
tert-butyl-ti-iphenyl-methyl, dcumyl-triphanyl-methyl, diphenyl-methyl-
triphenyl-mathyl. They are easily separable solid products. From among
the liquid peroxides the peroxide of tert-butyl-l-methyl-cyclohoxyl could
be obtained from tetra-(tert-butylperoxy)-silane and I;mothyl-eyolohexanol
In pure condition. The reaction of tetra-(tort-butylpe oxy)-silane with
trimethyl carbinol, and dimethyl-phenyl carbinol proceeds in an analogous
Tay, 'but the ROORI-peroxides do not result in pure condition. The
heterolytic reaction of silicon peroxides with tertiary alcohols in the
presence of acids takes place according to the equation
4ROH + Si[00C(CH 3)314 "H 4(CH 3)3 COOR + Si(OE) 4in the case of tetra-
(text-butylperoxy)-silane, and according to the equation
ROB + (CE03 SiODR, BOOR, + (CB 3)3 SiOH in the remaining trimethyl-
(aralkylperoly)-silares. The synthesis of ROORI peroxides does not require
pure sillcon peroxides as starting material which simplifies the reaction.
The well accessible tetra-(tert-iutylperoxy)-silane "may be of some
interest for synthesis". There are 11 references: 1 Soviet, I US,
Card 2/3
85478
Reactions of Silicon Peroxides 'With Some S/079/61/031/001/010/025
Tartiarg Alcohols 3,001/3C66
6 British, and 3 German.
ASSOCIATIOV: Belorusokiy gosudarstyennyy universitet i Institut fiziko-
organicheskoy khimil Akademii nauk Belorusskoy SSE
(3391orussian State University and Institute of Physicoorganic
Chemistry of the Academy of Sciences Belorusskaya SSR)
SUBMITTED: FebruaTy 18, 1960
Card 3/3
OL"'DFK-')P, Yu.A.- SFEVICIMNYO, A.N.-, ZYA'~IVDV, BYLINA, G.S.; YEVNIT"Aly,
A.P.
Diacyl peroxides. Part 1: Synthesis and properties of nonsymetric
diacyl peroxides. Zhur.ob.khlm. 31 no.9:29C4-2910 S 961.
(111RA 14:9)
3. Belorus~kiy msudarstven univprsitet imenj V.I.Lenina.
llhroxidcB)
OLIDEEKOPj Yq~,A N.,, akademik;
-.;-MlSEMHUKj X.L.; SEVCHENM., AJ
----`ZlATIXOVj I,F.
3.p'l-BiB-acylperoxy~-dicycloboxyI peroxides. DAL AN SSSR
.139 no.50M-23.20 Ag,, 16:1. (MIPI 24:8)
IS -'~-Tzvtitut fiziko-organicbeakoy khimii AN BSSR I Boloruaaki7
Zovuaar,9tve=7y uni-7arsitet im. 7,1..Ienim. 2. AS BSSR (fDr
Sevahenko).
(Peroxides)
OLIDEXOP, Yu.A.; YjAUNINA, A.11.; SIIK'InR,$ S.A.
New mathcd acid chlorides and acid bromides
of armatio acide. Dokl. AN SS'~~P -139 no.6.1383-1385.Ag 162a
(MIRA 34-8)
1. Belorusskd-y sgosudantvennyy univenitet im. Vol* Unina.
(Acids;p Organic)
(Halides)
OL:DEKC)?.,-lu 6~1 > N.A. .
Methyl mercury pentachlorphenolate, a new fungicide. DAI.A.31 BSSR
6 no.2:107-108 F 762~ OMA 15:!2')
1. Lmtitut fiziko-organicheBkoy khimli AN BSSR. Pxedstavleno
akadez-lkon AN BSSR B.V.Yerofeyevyz.
(Idercury organic compounds) (Fungicides)
OLIDEKOP, Yu.A.; NAYYER, N.A.
Photorsaction of mercury caprata. Part 2. Zhur.ob.khiz. 32
no.5:1441-2U3 )V 162. OMU 15:5)
1, Institut fiziko-organichesRoy khWI AN BeloruBskoy SSR.
(Decamolo acid) (VArcury salts) (YhotoDhe-mistry)
MY"ZRI N.A.; GE3ELIBMG, V.I,,- OLIDEKOF, Yu.A.
Photareaction of =ercury (11) "mn--oat t-3 -and ~x --napbU oat Le. nrurr. n1b. -
'"hin
Ir . 32 no.&2030-20.33 Ja 162. (1-11W, 25:6)
1. Institut MUlco-orgmUcheskoy khinii Akademil nauk Belorusshoy
SSR.
01'4ercury benzoate) (Mercury naplithoate) (Fhotoclienistry)
3/046/63/027/001/017/043
BI 63A1 8 0
AUTHORS: Sevchenko, A. N. , Pj!~ek~0_7141 yattkov, I. P., and
Bylina, G. S.
TITLE: Use of vibrational spectra for the investigation of the
reaction nechaniBm of auto-oxidation
PERIODICAL: Akademiya nauk SSSR. Izvestiya. Seriya fizichookayn,
v. 27, no. 1, 1963, 41-44
TEXT: Tn a spectrophotometer VIKC-14 (IRS-14)s the infrared absorption
spectrum of a reaction mixture of benzaldehyd.e and CCI was recorded
luring consecutive stages of the reaction in the range 700-2000 cm- 1.
After the end of the auto-oxidation, the absorption bands of a residue of
non-oxidized bennaldehyde and of perbenzoic and benzoic acid vere'found,
but no evidence for the presence of any other intermediate products.
During the reaction, ho-hever, bands with maxims appear 2' 852 cm-1
6 and
1255 cm which belong to neither perbenzoic nor ~en2oic acid. It is
assumed hat these new bands belong to some unstable intermediate product
Card 1/2
S/046/63/027/001/017/043
Use of vibrational spectra for the B1631BIBO
precedine.the perbenzoic acid. This paper vias presented at the 14th
Conference on Spectroscopy in GorIkiy, July 5-12, 1961. There are 3
figures.
ASSOCIATIONT: Belorusskiy gos. universitet im. V. 1. Leninn (Belorussia~n
State University imeni V. 1. Lenin)
Card 212
OLIDEXOP) lu.A*; SENCRAO) A.11.; ZYATINOV) J.P.; YELIMTSM, A.P.
.- I. -; ~... -11. 1-- ~
Acyl poroxides. Bart 2,7 Synthesin and propertleB of allphatle
nonBymetrical diacyl peroxideB with unbranched chalm. Zhur.
ob. khim, 33 no.W771-2774 Ag 163. (MIRA 16: 11)
1. BeloruBskly goBudarstvennyy universItat imeni V.I. Lenina,
CLIDEIDP, Yu.A.; MAMR, N.A.; PSIMINICHIM, V.N.
Acyl peroxides. Part 4: Reactions of methyl radicals with mercury(l)
acetate. Zhur.ob.khim. 114 no.1:317-320 Ja 164. (MIRA 17:3)
1. Institut fiziko-orqanicheskoy khimli AN BSSR.
SEVCHMO, A. M.; CLIDEKOP., Yu. A.; ZYATIXDV, 1. P.; 3311N.A., G. S.
I,hm of ribration apectra in, atuayirg the meebanbm underlying
melf-axidation reactions. lzv. IN SSSR. Ser. fi2. 27 no.l:
42-AA Ja 163. WRA 16-.1)
:1. Belvrusa3d7 gmudaratvenmyy univaraitet in. V. I. lanina.
(mo:lecular spectra) (oxidation)
?j.A. Lllaorp .,.A.]; EM,1;21p AsAw; UFsiim., Fez. [uni::i-tzi, F-Z.];
MYM" CLiDEKC)P. -du.A. LA-17dekopy TU.A. I
f M(,r, 'vent5a
Daconpo5itlon of PheMY1 &O"ta" 0ury rxida ill volu
nave noal:49-54 364
V--St:31. PIT BSSR Ser. (t-111RA 17%7)
ACCESSION NR3 A?4"1 0926
M.9101713a Olldekop,, Yu. A,; By*lina, G. So
310250/64/DOB/005/0316/0320
TITLEi TIhe initiation of styrene polymerization by homologs and substitutes of
acetylbeiizoylparoxide (Presented by Acaducioian No Fo TW=1DAkD)
SDURCE: AN B5SR. Doklady*., v. B., no. 5., 1964., 31&320
TOPIG TAGSi styrene polymerization, acetylbenzoylparoxide ~61ymari2ation initiator,
acetylbenzoylperoxide homolog initiator., acetylbenzoylporoxide substitute initiatc;
ortao substituted acetylbenzoylparoxido, meta substituted acetylbenzoylperoxide.,
para substituted acetylbenzoylparwdde, styrene pDlymarizati-otrat9j, polynarization,
activation energy., Flammett, equation
XSWRACT: The initiation activity of 18 acetylbenzoylperoxides on block p6lymar_
ization of styrene was studied, The polymerization rate,, determined dilatomet-
riml_~y,, was used as a criterion of initiation activity at 60., 70., and BW in the
presence of 0,015 mole/titer of the initiator. It was found that the polymeriza-
tion rate inoreased with temperature, and that the substitutions in the orbho
position in. the benzene ring had an enhancing effect'on the polymerization rate of
styrene, Tbia was true regardleaD of whether the subAitute was cblorine,, bromine.,
'Card 1/2
=EmioN NR, AP404o926
a methoxy., or aceto)7 group. The substitution of electron-acceptor substances in
nots. and para positions showed an i:T~Abiting effect on the pblywrization rate of
styrene, while alsotron-donor substitutes enhanced it, (but to a lwaser degi*o unan
ortho-substitutod acetylbompylpercoddes). The affect of substituting in mots,
and para position on the performance of acety3benzoylperoxide as initiator,
correlated van vith Hammett's equation. * It was found that extending the length
It of the hydrocarbon chain in benzoylp6rcoddes caused a gradual lowering of their
initiation activity, Orig. art. bas3 3. table and 2 charbis.
A=IATION3 BelorusBki:7 gosudarstvenn~V universitat Im. V. I, Lenim
(Bolorassian State University)
SURETTIM3 32Ju163 ML 3 00
SUB COM 00 NO IM SOV: 012 OTIM: 020
Cord 2A
CLIDEK%-)P,, Yu.A.; KALRIIIIA, A.1,11.
Thermal reactions of polyhalomethanes with aldehydes. Zhur. ob.
khIm. 34 no.10:3473-3478 0 'C-4. (MM 17:11)
1. Belorusakiy gosudarstvennyy universitet im. Lenina.
OL'EEXDPJ, Yu.A.; YELINITSKIY, A.P.
Study of acyl peroxides. Part 5: Preparation of sy=etrical
diacyl peroxides from asy=etrical diacyl peroxides. Zhur.
ob. kbim. 34 no.10:3478-3481 0 164.
(MIRA 17:11)
1. Belorusskiy gosudarstvennyy univernitet im. Lenina.
~l
OLIDEXOP, Yu.A.; BYLT`;A, G.S.
Acyl parcxiae3. Part 6: initlating activity of asy--Z-atrical clacyl
peroxides in th bulk poly--erization of styrene. Vysakem.so-ed. 6
no.921617-416-13 S 164. (MIRA 17:10)
1. Belonisskly gosudarstvennyy unliernitet Imeni LanIna.
-0~1-11DEFMP; Yu,A.-, MAYTER, N.A.; FSHEMACUNTI, V.N,
Acyl paroxiden, N-rt 8s Rgactions of phenyl radicals with r4rcury
(T) acetate. Zhur. ob. khi-m. 35 no.5a904-907 My 165. (MA 18:6)
1. Inttitut fl2lklv--Drgarlchaskoy khimil AN Belorusakoy SSR.
7--
ACCOMOU NR ALF-51~ 15 2 3 5 UR/0286/65/OW/009/1-~
AUTRORSj 01 dekop, Yu. A . 7-nt~,erc-' r , 7,
TITLE: A method for oltgouier pro-aticto. Class 12, 110, 170486
SOMCEt Byulleter.' '11-.-;,~-,..im:jkh1 mirU~ov, no. 9, 191j5, 20
TOPIC TAGS: tetradi'
aceV1 perox~Jde,
05TRAM This Aqthor a method for Obtaining ollg-vwr
tat-bloropentall land rionan h! ro
,3uch as an ie c o butane. TetracMorethylcme rPR
T.'~7
--axide whilc -m-med. TTj eriana 8o produoed is subsequar,`.'
aceV1 per e
'with water, d-riwd orith --PLIc,un nhloridp, sops~.rated fr= the solve-at,
in a vaau=,
'ASSOCIATION: none
SUMD7?M)t 063op63
:NO MW ScAr - 000 "-"11i I CM
Cay'd 1/1
M
IS WIN W
l
l w
-OLl.l;EKlq?,,,-Ya,,A,4 BY1.1NA, G.S.i GlIAOVICH, L.K., BULOYCHIK, Zh.l.; TEYF, Zh.D.
Acyl peroxides. Part 71 Synthesis of asymetrical diacyl pe-Tcxides cl
allphatic and hex ahydroaralypha tic series. Zhur. arg. khim. I nc.li82-
86 J a 16 5. (MIRA 1815)
1. Bcaoruss-kiy gosudarstvemirj universitat im. V.I.Loni-na.
ULIDEXCP, Yu.A.; KOVAIE'VSUIA, A.M.; SHKLYAR, S.A-
TherrAl reactions of carbon tetrachloride and brmotrichloro-
methane with organic acids. Zbure orge khime I n0.9:1540-1544
S 263a (MIRA 18:12)
1, Institut fimiko--Drganicbeskoy kh:Lmii AN Belorueskoy SSR i
BeloruBski-y gosudarstvemnyy universitat imeni V.I. LBninn.
Submittea November 23,, 19E4.
yu.-.; CH*~RKII"~, L.A.
Dinulfo derlwates of di-tpr-tr.Aylperoxide. Zhur. org. khirl.
no.1,1:1563-156? F) 165. (MIRA 18:12)
1. Institut fiziko-crganicheBkoy fiziki AN Belorusskoy SSR.
Suli-Attlud June 22, 1964o
peroxitli- ivlth a,:~yl cYI~,rldes and k,3toncs. t"h u0
I i-ic).'lliI934-1936 N '65. (Plipt l&12",
klilmill Vtlorusskoy
5-3700, 5.3400 77405
SOV/'79-30-1-66/78
AUTHORS: 01 Idekop, Yu. S., Mayer, 11. A.
TITLE- Photochemical 11,~~actions of Mercurous arid Mercur',Lc
Acdtate and Mercuric Propionate '
PERIODICAL: Zhurnal obahchey khimil, 1960, Vol 30, Nr 1, pp
303-307 (USSR)
ABSTRACT: Photoche,-nical decarboxylation of mercuric acetate
in benzene, acetic acid, and their mitctures; of
mercurous acetate in acetic acid; and of mercuric
propionate in benzene and acetic acid was investigated
in this work. Experiments were conducted in a
quartz flask proxided with a reflux condenser and a
bubbler. A PRK-4 mercury-arc lamp was sealed *
horizontally into the flask at such a level as to be
iranersed into the reaction mixture (0-03 moles of
salt in 150 ml solvent). The evolved gases were
collected in a gas burette, connected with the
Card 1/4 reflux condenser, and analyzed on VTI-2 and Hh-IM
r1hotochemical xiieaction3 of 14;-rcurous 77 110 5/
a nd Y 0 '/7:'
iorcurlc Aoetate and Me~rcurlc Prop 1. onal te- SOV/79-30-l-"o/
C--a rd 2,14
gas anatlyzers. After cool Ing of thereaction. mass,
the solid product,-~ were washed with benzene or
acetic acid and arvalyy~,,d. The product analysis has
-ho,.-in th-at: (1) Photochemical decomposition of
mercuri(, acetate and proplonate in benzene results
in formation of mercurous salts and compounds of
the type RjjrrOC0R(wIhor(I R = CH or C H ), their
C, 3 2 5
respective yields I)eing 60-68, and 30-34%. Both
Zalts are stable to irradiation in berizene. (2)
Addition of acetic acid speeds up photodecomposit ion
of (RC00).Hg with increasing yield of R11grCCOR and
a decrease in yield of RCOOI~,!; soine metallic mercu.-y
is also formed. (3) After irradiation of mercu-ic
and mercurous acetate in acetJc acid and mercu--ic
propionate in pv6pionle '.-tcld, mctal2ic mercury and
compounds of the type RHCOCOR (in 6o-68% yield) were
obtained. The latter ave d-.~composed upon prolonged
Irradlation with form:ttlon of inetal-lic mercury. (11)
The gaseous, producto wu-re: meth;Lno, ethane, GO,,,
4.~
Photochemical Reactions of Mercurous 77405
and Mercuric Acetate and Mercuric Propionate SOV/79-30-1-66/78
and CO from Hg(l) and Hg(11) acetates; ethane, ethylene,
butane, C02, and CO from ng(II) propionate. (5) On
the basis of these results, the following scheme was
Proposed for the decarboxylation of rw-,4rcuric salts:
HIE is
b.-drogen-
containing
compound
llcoollgoco!i -h", Hcoo - + .11gDC011 0)
(R-C11, CJt C.11.)
KOO - 11. + CO, (2)
fl. + .11gocoll --3-. 1111gocoll (3)
11 - + 11C0031gocoll B11gocon + TIC00 - (4)
F1 - + 11,11 11 H + W. (5)
2H- B-11
< (6)
11+21 + n-11, (FAA n = C'11.) (7)
2 - 11SOC031 JISI(OCOIJ), 0)
11gstocoll).2 - 13g + Dgtocoll).S (9)
Card
Photochemical Reactions of Mercurous 77405
and Mercuric Acetate and Mercuric Proplonate SOV/79-30-1-66/78
ASSOCIATION:
SUB14-TTTED:
Thus, alkylmercuric salts (RHgOCOR) can be conveniently
synthesized by photochemical decarboxylation-of
mercuric salts of aliphatic acjdS.
"00 - ---3- 11C0 - + 11202 (10)
11co - B - + CO
There is I table; and 7 references, 6 Soviet, 1 German.
Institute of Physical Organic Chemistry, Academy of
Sciences, Belorussian SSR (Institut fiziko-organicheskoy
kh1mii Akademii nauk Belorusskoy SSR)
January 14, 1959
card 4/4
and application of cpti=am nonlinear
avtomat telemekh no. 1:7-24 Ib4o
OLIDENBORGYR, A.A., veterinarnyy vrach (Gomel')
- .-I-.- -- - 5~~
Characteristics of the course of rabies in swine. Vetarinarila 39
no.1:30-31 Ja 163. (WRA 1616)
(Rabies) (Swine-DiBeases and posts)
UlDlDmMJ6 GIB.
Superregenerati-re recelTer using a squitter cira-adt, PadloteMm3ka
8 no.4j27-38 Jl-*-~ '53. (MIU 11:6)
(Rmilo-Ilecel-vars and reception)
0 N - r V.1 I, po: r LO
t tALo-ILUL
P:.j "t v
9 Iv Polm h ii h -.k4
t t. n cd c, ja trt,li I ~, i
Vunctional zchcol of et nojr,-~phy In service c, --ritisti in-,Trialism.. Trudy ln~t.
I th
XN S:~.;h 12, l)-51.
9. Monthl List of Russian Accessions, Library of Congress, "arch. -1951, Uncl.
2
I'; -v
4-11BY . -ice
mlaynn spten rf kin,:;'Illp- TrulY 'A" 0"'~Sji 14, 1951.
y
9. Monthl List of Russian Accessions, Library of Congress, April 1951, U'cl.
2
Sudan - 7"'t!Lnclcgy
Crigin of th!! ptople of tjr!~ centril Stylan frcn ti(-. ancient hi-story oll th'~, F;riu~,a-kctckc;
language T--I,CL;Ds. scv.,--.tn. -C. 2, 19~2.
Z> - i
9. Mon-thl List Of Russian Accessions, Library of Congress, Septemb?!r - 195Y, Uncl.
1. OL-IDE11CCARD T), A.; PCTEM-Ml' 1. 1.
2. USSR J600)
.4. Ethnic 7~rpes - Africa, West
7. Ethnic composition of the present-day ?opulation of Western Equatorial Africa.
Sov. etn. No. 1, 1953.
1 1953, Uncl.
9. Monthl List of Russian Accessions, Library of Congress, April
OLIDAROGU, D.A.
I - I
.Antiquitiefi of 3amin (an the 'basID of Collections of the XUDOun
of Anthroyoloo and 3thnography), SborAussan'tvi sin. 15:357-410
'53. (Mak 7 -. 4)
(Benin, Iligeria-Antiquitles)
OLIDEROGGE, D. A.
17-?,
9 Sixth International Congress on Anthropological and Ethnological
Sciencps, Paris 31 JuIY-71 August 100.
7TRAITS :-ZSErjT1M DF VE-VOLUT1,Y) DIZ SYBTi)~~ DE FAaE:Tj-.E11
OLTEMI-XG.Ell D". -11.
0.........
"0 r
'pisatellnyye sistem:j radstva Za-padnowo Sudania.,
report submitted for 7th intl Cong, Azithroj)ological & Ethnological Scienceo,
Moscow, 3-10 Aug 614.
OLIDEROGGE, G.B.
.
Certain special mathematical correlating codes. FL-adlot--Y-tnika 3-8
no.7:14--I JI 163. (MM 16:10)
1. Deystvatellnyy cblen INauchno-tekhnicheskogo obBbebestva
radiotekhnl-ki i elektrosvyazi in. A.S.Popova.
'AtTMION NR. AP501 303 U H,:1C i 6 5 G 1) 0.1,'() 0 5.10 0,5 111/ "i`~'
6 1 . ~ 9 117 16 Z 1, 39 1. 154
AUTHOR: MeVnikov, y1j, IN, 01'derogge, G. D~
TITLE. Some problerns of noire im-nunity of digi t-al-info rmation trami.-n-
under gkoup-error conditions
SOURCZ; Elektroswjaz', n,).
TOPIC TAGS: digital mforrnzt!on,
immunity
'ABSTRACT: T-lic aseccultion ;s :onsc,,,i.,t~red the noise-inirivw.,A,
ment and the le-nijuh of a sagnit-rit kvor~!, metisage);
length of a group erior or,-cir --btribjt',on. The nciv;e
(cliannel) i9 evajaptc,i as a probab;'k-ity 0! p--~~sv "i~ atortion ancl, tht. cu
.distribution of the lengi-11 01, group errort;. F(jrrnuias for estiniating ~hw
probabi.Uty, with a knawr distribution of the length of waffunrtion grcrup-ia
Card.- I JZ
presented; the formuiae are valid ftur- I-Ij~v _~v, r;lf er.--
probability of distortifg t~ie d)git i~- lute r-,,It-tc.-i ~..r Y,-rDs, M_illgc), A-
KiD6PjeXtran8I-Id86iD.I gyfftOMA CiCGcribed bv A~ V. Yontain and R, C-1- C~.ii
-IRE,_ ta, 6). W~~th a group ~,,rror 0;mtribution, the ufle 'A
codes i e ent b e C 7, L, 6 e, 0EC' r e dUn 11 L,'! C V A j~, 9 C~ C-txf-e-d With S'If-ch f-c-dr'p 1-
such an incre ase in tho prohab, 1~ty ol dLstc;rt~on Linat it cannot be off'-jet,
correcting ab"Ifty. The rise of errar-detect;ng coden and the repet~,,,-.ov
ffmanages on request iaeema to be more prorni ni rig. Orig. art. hao. f i
16 formulas, and 2 tableA.
A
SSOCIATIOM none
;hUBMITTM, 130ct64 ENCL: 00 SUB CODE: E,"
NO REF SOV: 00 Ir OTIMR: UOZ
ICard 2/2
i-17,
L I I;Z`~-
USSR/Sle CtrL city
Cowdal 1JIMe3
Naves, Electro:-ia~-netic
i-iar/Apr Lg~,~
nTi:eo2-j of Coa:Ndal Spiral Lines," L. 11. Loshakov, Candidate Phys Tech Sci; Ye. 6,
013dero-ge, 10 pp
'j' diotekh" Vol Ill., No 2
Ra
Gives approximte theory of distribution of electromagnetic waves in spiral coaxial
line, and establishes method to calculate dependence of phase velocity upon geopletry
of the line and tll,,e frequency.
YA 51!f7
UW11-RAdio Recepticin
[~ Zeneratorm
Ncy fDoc ~ 48
-9'A:C;=-tribut1an tc, the Problem of Utilization e. a
Supwrgenerator in a Nonlinear System for 'Reception
of'7~rrequf,ncy-Modulated Signals," G. B. 011derogge,
Bbsr PP
-Ra-itotaki, " vo,- iii, tic 6 7 1
ZZ&mJ_-.es basic relatimshIps shar&cterizing opera-
tlc= of supergennerator with Its circuit slightly
out of tune with "he frequency of the signal being
rocel-red. Shows that the supergenerator frequency
4*ir-s not app6ar in its oscillation spectrum de-
the fact that the instantaneous frequency at
ajar given time Is, equal to the supergenerator
40149T99~
U=ARMUO ftception (Contd) Nov/Dec 48
fr*quency. Exammines problems of supergeneratcr de-
tect:Lng and amplification of frequency-modulation
Oat-11-1-ations. S~=Itted 23 Jul 47-
rm 3M
3OL4
Q
LUTHOR LOSILIKOY L.311,,Regular Uembox of Society OLMEROGGE Ye.B.
TITLAO ?ast'ffaves in a Coaxial Sj;iral Line.
(Bystry7e Tolny T koaksial3noy Bpixallnoy linii-.Rus3ian)
PERIODICA1 Radiotekhnika, 1957, 7ol 12, Nr 6, pp 25 - 30
ABSTRACT An approximate theorotical InTestigratioD of the propagation of fa3t
'Waves of various kinds in a coaxial s*al line Is carried out. The
conditions under vhiob such a propagation Is possible are doterml.,
mad. The analysis is carried out within 'the frame of idealizatior,
I.e. the spiral is replaced by an anisotropically conducting cylin-
drical surface with a radius zimilar to that of the average spiral
radiuz. First the initial relations and then the equations for the
phase constant and the critical frequencies are found. ?or the yur-
pose of simplifioation of the calculation an ideal conduction of
the sl*al as well as of the scraen are assumed. Six independent e-
quations are formed. by means of which 5 of the 6 integration con-
stants of the equations for -the fields can be expresBed by one- A
Transeedent equation is obtained required for the yhaue constant
B
of the waves of various types, which Can propagatg in thiD lint-
M
Investigated. The datorzinstion of the phase constant D
, leads to
,
the graphical solution of the transcedent equation for the gi7en
geometry of the line as -well as of the frequency. The equation
for the critical frequencies is obtained and the evaluation of the
roots of this equation shows that the basic types of the wavea, in
Card 1/2 the line investigated which have the lowest frequency are the a-
I ,
V
t". I-J)
MASE I BOOK EXPLOITATION SOV/5292
Konferentsiya po elektronike sverkhvysokoy chastoty
Trudy (Transactions of the Conference an Superhigb-Prequency Elec-
tronioB) Moscow, Oosenergoizdat, 1959. 271 P. 3,500 copies
printed.
Sponsoring Agency: Vseaoyuznyy nauchnyy sovet po radlofizike I radio-
tekhnike AN SSSR.
Eds. (Title page): 1. S. Dzhigit, Professor, and Ye. G. Solov'yev,
Candidate of Technical Sciences; Ed.: S. Akalunin; Tech. Ed.:
,0. Ye. Larionov.
PURPOSE: This book is intended for scientific and technical personnel
concerned with the development and operation of superhigh-frequency
devices.
COVERAGE: The book contains a number of papers dealing with the more
important problems of siiperhigh-fraquency electronics. The papers
Ca
TranBactlons.of the Conference (Cont.) SOV/5292
.011derof,'ge,_Ye. B., and L. N. 1.4Bhakov. Computation of the Coupling
Fact-o-r,n a Ri-fildr-Belix Backward-Wave OBeillator 23
Sol,ovlyev, Y,e. 0. "Counter-Line StratcherB In a Rectangular Wave-
guide" Delay System 35
Silin, R. A. Analysis of Multistage and Polyserial Line Stretchers
of Delay Systems 45
AfonBkaya, M. N., V. 0. Gabyshev, A. S. Dunayev, S. A.
ZuBmanovskiy, M. L. Lyubimov, A. 0. Mishkin, and 0. P. Shchelkunov.
Klystron Amplifier of the 10-Centimeter Band With 20-Milliwatlt
Pulse Power 58
Oveharov, V. T. Cylindrical Electron Beam in a Uniform Magnetic
Field 80
Xozell, 1. Sh. Concerning the Problem of FocuBing a Cylindrical
Hollow Electron Flow in a Periodic Magnetic Field 90
(;JjjP,fit._W5 2,
SOV/,P9-4-6-10/27
AUTHORS: StDllmakh, N.F. and Ollderoggt, le.B.
TITLE: Propagation of Electromagnetic Waves in Corrugated Systems
-C,
ifith Annular Slots (Rasprostrananiye elektromagnitnykh
voln v diafragmi.rovannykh zamedlyayushchikh sistemalffi s
hol"ta-evymi shcholyami)
PERIODICAL: Rudiotelchnika i eleUtronika, 1959, Val 4, Nr 6,
pp 980 - 987 (USSR)
ABSTRACT: The systems considered are shown diagrammatically in
Figures la and lea. It is assumed that in general the
inner periodic structure can be displaced (along the
axis z ) with regard to the outer structure by a distance
L . It is further assumed that losses in the conductors
can be neglected and that all the time functions are sinus-
oidal. The system can be analysed by using the method of
-the Upartial regions" (V*M. Lopultbin - Ref 6). Tt is
assumed that in the re,&;Loxx1 and III (Figures 1) only
radial TEM-waves can propagate, *While in the region 11
a TM-wave exiBts whose dependence on the co-ordinate z
Ir- in t-he form exp(-Jp z) a The fields in the region I
tJ'.4M% (1). In the region 11, the fields
Cardl/4 Dky y 19
S017/109-4-6-10/27
Propagation of* Ele;;tromagnetic Waves in Corrugated Systemn with
Annvlar Slots
are expressed by Zqs and (5). For the region III
of the oorrugated waveguide (Figure It ) the fields are
expressed by Eqs (6) and (7), -while for the coaxial
corrugated line (Figure is) tha fields are-expressod by
Rqs (8) and (9). The boundary conditions for a slot
denoted by the number q can be expressed by Eqs (10)-(15).
The boundary conditions are u5od to evaluatb the integration
constants in the field equations. The constants are
defined by Eqz (14)-(21). The dispersion equation of the
systems ia in the form of Eq (26), where the varlous
paramaters are defined by Eqs (27)--(32); the parameter a
for the waveguide is given by Eq (32), ithile for the coaxial
line it is defined by Eq (33). The solution of Eq (26)
can be found graphically by finding the intersection points
of the left-hand side and the right-hand side yarts of
the equation. The coupling coefficient between the n-th
spatial harmonic of the elettron beam iv d*finod by
Card2/4 Eq (34) where B zn is the longitudinal component of the
sov/iog-4-6-10/27
Propagation of Electromagnetic Waves in Corrugated Systems with
Annular Slots
clettric field of the n-th harmonic and P is the power
flow through the system (-without the beam). The final
expression for the coupling coefficient is in the form
of Eq (39). The theoretical results are employed to
evaluate a number of curves illustrating the performance
of the corrugated system3. The results are shown in
FigurO3 2-8. Figure 2 shows the disperAion curves for
the first background harmonic. Figure 3 1 'Ilustrates the
dependence of the first backward harmonic on the wavelength
in planar and coaxial systems. The dependence of the
coupling coefficients and the density of the starting
currents on the parameter (3 = DP/21Y is illustrated in
Figure 4; the solid curves give the coupling coefficient
while the dashed curves illustrate the current densities.
Further dispersion curves are given in Figure 5, while
Figure 6 illustrates the coupling coefficient for anti-
symmetrical waves. The distribution of the electric field
in the annular slots is illustrated in Figures 7 and 8.
Card3/4 From the analysis, it is concluded that the symmetrical
SOY~~Og--4-6-10/~7,
Propagation of Electromagnetic Waves in Corruga e ysteTas With
Annular Slotts
wave3 can propagate in a coaxial corrugated line only
within a narrow band; the an-ti-oymmikitrizal -wavaas can
y one symmetrical '%,rave type
propagat6over a vide band. Onl-
can exist in a corrugated waveguid-3. Tbo displacement
of the two periodic structuros (the inner and the outer)
-with respect -to each other has no significant effect on
the shape of the dispersion curves in both the corrugated
zyztems. Thero are 8 figures and 9 references, 6 of
which are Soviet and 3 Bnglish; one of the Soviet references
is translated from English.
SUBMITTED: 'IMarch 7, 1958
Card 4/4
88698
S/()58/60jft0A10/0O7/0 14
C71 Z/ 23 ADOI/A001
Translation from: Referativnyy zhurnal, Pizika, 1960, No. 10, pp. 3D9-3)D, # 21~27
AIMIORS3 Ol'derogge, Ye.B., losbakov, L.N.
TI Calculation of Coupling Coefficient in a Backward-Wave Tube With a
Double Spiral
PERIODICAL: Tr. Xonferentsdi po elektronike SVGh, 1957, Moscow-Leningrad, Gosen-
ergoizdat, 1959, pp. 23 - 24
TEXT: The authors derive a formula for calculating the coupling coeffi-
cient X. for the Interaction of an electron beam with a field of arbitrary space
harmonic In a backward-wave tube with a double.spiral. The spiral Is assumed to
be of the strip type, screen effect and losses In the spiral are neglected.
NumerIcal calculations of X are performed by the formula obtained for a number
of particular cases. it tucned out that the way of.current distribution over the
spiral strip affectsthe magnitude of Kc only insignificantly. X.-values decrease
sharply with the increasing number of the harmonic. The coupling coefficient of
the first reverse harmonic, X.-1- was Invtstigatod in detail. 7he graphs of )1c-1
Card 112
A8698
S/*058/60/OWA 1O/W7A 14
AOOI/AOOI
Calculation of Coupling Coefficient in a Backward-Wave Tube With a Double Spiral
are presented as functions of geometr7 of the spiral, frequency and dimensions of
the beam, which are of Interest for the selection of characteristics of the back-
ward-wave tube. It is found out that there is an optimum value of the Spiral
pitch, corresponding to the X,_, maximum, for the fixed values of frequency and
radius of the spiral. It Is mentioned that annular beamB are expedient for the
operation of backward-wave tubes at sufficiently low voltages. Spirals with
relatively large diameters can be used in this case.
0.N. Shvedov
Translator's note: This is the full translation of the original Russian abstract.,
Card 2/2
A C C F-55 ION NR - A P S-C " 081!b 3,"D I 8/007j00
AUTHOR: 01 Ide-rogge, -G. B. (Member of the Society, see "Association")
TITLE: SOMC SPCCiAl niatrix-type, corroctive code-a i.j
SOURCE: Radiotekhnika, v. 18, no. 7, 1963, 14-19
TOPIC TAGS: corrective code
4.
4
ABSTRACT: A square matrix consisting of two-digit elements can be tyT~n;i
formed into another sqizare rnatrix whose rows and colurrins do no' (owil',
numbere of the corresponding rows anc, collun-nfj of the original rnatriy,.
transformed matrix is cah'ed the "Euller's square. " The article consider a
correctIve binary codes whose control symbols are formed by making evrn paz-
in the rows and columns of Euleria Bquares. The suggested codes permi,
detecting and correcting single, double and triple errors that occur in
rrdtting in-formation &long a symmetrical channel and also perrnit detectln,:
i Card I /Z
L 1)1923-63
ACCESSION NR: AP3004086
quadruple errors. It is pointed out that the new code is close to optimuni itp f
as t1te number of resolved code combinations is concerned. Orig. art.hz.8.
10 formulas.
ASSOCIATION: Nauchno-tekhnlcheekoye obahchestvo radiotekhniki i
elektroavya--i %'Scientific and Technical Society oi Radio Engineering and
Ele ctrocommunt cation)
SUBMIT-TED: Z5May6Z
SUB CODE: CO
DATE ACQ-. 05Aug63 ENCL: 00
NO REF SOV: 00 1 OTHLR: 000
Cori
jU2*42 bVT(j)/EW(b)-2/FWA(h) Pm-4/Pu-4,/Pac-4/Peb/Pi-4/PJ-4 Jill
ACCZMONKP-, AP501G-100
AUTHOR: 1,oshakov., L. N., 01'derugg
,e, Ye. B., Pchel'riikov, Yu. N.
TITLE: Possibility of obtal.ning x neg;ALVve depre9llon factor in TW tubes
(Reported at thm Internat4onai Vocroway,.
SOURCE: Rad;otekh.mlca elc-Ittrar.-Ka, 1,C), ,e. 4, !'965, 681-688
TOPIC TAGS- tUI)f
ABSTRACT: It was statf,,~': ~r-- ptevioi-s akolio-, r' works (Rad. i elektronika.
5, 1z, 1968, and IQ5',~, ,i. 0-,at, ~-icllr,~ certain c(-)ndi'LLon[,, the
depression facwr r- in xA valur~, Vh~-
article considE~r5 a p-?.rt~ !-!C" (- "Abu
_1o'se. to; tlic
and the argurnents of the ~tfi -twil are qmall- k) O-IJ6 c-ase, dit tr~in-
acendent diaperipion vquialirl[) f !)
of the TW tulbc mily be npprocciniately
f.:mLsfarmed into an algebrai( charracteriotic equal:znii of tho 4th degree.
;Card 1/2
'_ L 49M, -.63
'ACCEMONNR: AP5010100
of the latter yields this formula Pir the depression factor:
In 1,12
1., 12
whose values may be negative. Peculiarities of behavior of the TW tube, un'!~-,
negative r conditions, are analyzea by a nurnerical Polution of the characver r..
equ^tton. In addition to the usual field arnplif- cation, the TW tube, when itFs
felectron velocity is varied, may amplify the space-charge wave without takin,
I power from the electron boam. Orig. art. has, 5 figures anti 25 formuls.a.
I ASSOCIATION: none
I
SUBLUTTED; 16Mar64 ENCL. 00 SUB CODE: EC.
i NO REV SOV: 008 OTHER. 002
2 1 Z_
L 29197-66 JXT(EX)
'.CC NR: AP6008287
SOURCE CODE: UR/0109/66/oil/003/0503/0513
:AUTHOR: Loehakov, L. N.; 01'derogge, Ye. B.
ORG: none
TITLE: Calculating the coupling factor and depression factor for a ribbon helix
when the electron beam interacts with the field of one of spatial harmonics
SOURCE: Radiotekhnika i elektronika, v. 11, no. 3, 1966, 503-513
TOPIC TAGS: TW tube, electron tube
jABSTR-ACT: Design formulas are developed and some numerical values calculated
~of the coupling factor and depression factor for the case when the electron beam
Intoracts with the field of a spatial harmoaic in a ribbon-helix-type delay system.
7A dispersion equation is set up for a single- or multi-start ribbon helix placed in
a homogeneous nonabaorbing medium. Boundary conditions at the helix are
,Card'1/2 UDC: 621.385.6.001.24
L 29197-66
.7ACC NR: AP6008287
Jormulated according to D. A. Watkins ("Topics in Electromagnetic Theory, NY,
i:1958, P. 52). Finally, very complicated general formulas for the coupling and
,;depression factors are developed. Numerical values of both factors, for
:a/b a 0. 9 and 0. 4. aro calculated; a in the cloctron-beam radius and b is the
~helix radius. These values show that the deprousion factor for (a BW tube with) a
itwo-start ribbon helix is of the same order as the depression factor of an aniso-
,tropic conducting surface replacing the helix. Orig. art. has: 5 figures,
I
k58 formulas, and I table.
iSUB CODE: 09 SUBM DATE: 25Nov64 ORIG REF: 004 OTH REF: 00 1
iCard 2/2
,PPRICH, Eliaka; OTAKAR, -iarban
U2s of pv27est-er resins as casting and corrosion material
in anatomical prectice. Cesk. mort. 1-1 n0-3:286-288 163.
2. Z ana,tomickebo ustavu 193mrBka fakulty University Karlovy
v Prazza Jlrednoota: prof. MUDr. et TLNDr. L. BorovansV, SeDr.
(RESINS)
OTALAR, Marhanj DLDPJCB. Eliska
Imbedding of anatonica2 preparations into the "Din,, ChS
polyeBter 10,4. Cask. morf. 11 no.J,:372-373 163.
2. Anatonic]V uBta-7 fakulty vasobeensho :,LekarBtyi univarBlt7
Karlovy v Praze, prednOBta prof. dr. L. Borovans)7,DrSe.
(TWINS) (BISTOIDGICAL TECT[NICS)
+T.
01'DRZHIX,'.,Ooclok LOldrich, HodskJ, lmyh. (ChqkhoBjOTakjya)
Coal yreparation Im henTy fluldD at the Xomoram7 coal yreparation
3)1amt. DbDg. i brik. tigl. no.7:61-68 158. (MIRA 12:7)
(Cz9chDslova)da--Coal preparation)
=SION Mki AP4CW49937
AVMR. Oldrich. K. (Engineer, Candidate of detentes) ~_b
I TITL9: The 9TIA section
SOURC19i Listawny. Vyzkx=iy a Rkusobni letecky ustav. Zprevodaj valu, r~
49-50
TMC TAGS: comptiter center, date procesving center, aeronautical res~-a,
aviation indurtry, automtiot
ABSTRACT: On January 1, 1q62 the Vyzkurmi a zkusehni letecky ustaN, (Av~,, 1
arch arLd organized the Center for Infermation 'T'be
s
e
~Atofllot 4. on - sfti I,n-- D__rlie r to co-neentrate I tv workers and eq%tipment CJF.
automation and computer rechnLquee in the aviation industry. STIA n0%'
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card machines f or admInis trat i-ve opera t tans , rhese al I advi me ZT' ( f4(
of the CSM (C zeebb ~ lov-ak Be ien t i f i c - Tocfinits I Seri-ice) . ar r ange lie r 1
turae ancP help train thoir techniciants. BTU oleo conducte manth-lf or M~
expertv on Ppecif Ic phases of witomtion and computer work. Fol lovini, t h- em ~~7
is a description of the Kathemtice Refervnce Library (SM) publLzb*~.' iii i,-~
cmd 1/2
L 24742-0
ACMStOR NRt AP4049937
T~mwtgiz, Hoseaw, since 1%1, Its eight volumoo art listed, sveragin,,g 3fx
each, wW mcommondo4 for all research and development vorkers dealing krt~.~, v~izriw-
=ties.
AMCLATIONS oym
00 RPM.- 00 MM OWE- AC. IP
aw MI ow No
'Cod
0 11- D /,-' / _-_ ii,r
CZ=OSLOVAXI A/Chenical Technology. Chemical Products and Their Ap-
plication. Dyeing and Chemical Treatment of TextileB. B-34
Abs Jour: Referat Zhvar-lbimlya, No 5, 1958, 16567.
Author Mert Oldrich
InBt
Title Development of Mode:rm TecImology of the Dyeing of Fabrics
Part 111.
Orig Pab: Textil., 1956, 11, No 11, 338-340; Ifo 12, 367-369.
Abstract: Continuous methods are considered of the dyeing of fabrics
vith Tat dyes and direct dyes vhich are fixed vith co;per
salts or by means of dilazotization and coupling. The follow-
ing dyeing procedures are discuBBed: by J rsion, by im-
mersion and steaming, in William' chests, in fased metal.
Part I see MhXhiz, 1957, 49180.
Card : 1/1
GTRWHWI Vojtecb., prof. MUDr.Techn. spolupraceiDINTAROVA, hana; Q~PUCHJbca
T1,9 chLnge in the effrct of adre;inlin t~nfl noradrcnn-f-fn cr, thr;
Ucod pressure durimg the critc.-enesis in rats and its causes.
Sborn. ved. prac. lek. fak. Karlov. Univ. 7 no-42513-521 164.
1. Matodra famakalogle (pre&ostn: prof. YURr, V. C?Ty'nnnrunn)
Lelarike fakulty Karlovy UnIverilty v Ilmdel Kralove.
AIMHOR: Oldn-c~~, Poupe
A magnetuic v,-.Ih Dositive feedback and control-led
of disp--acemeri'~
FERIDDIUL: Referativnyy ?~hiurnui`, Avtomatika, talemexhanika i vychisl-it'ellna~~'
tekhnika. 1~ abstract ZX)i Xzachosl- Pat., 1C.1 ZIP--
T: 7ne Laxt a r a Traplogtic amplifier circ-,-
e:'
i.n' e r-.. a I f e ed ba c A i7- ~Lr '.c,.~il~ whan dasTx)tion
occ-,---s in ',he. ccmu'ec *"e(,
Vw 1 : 1,
ln'r Lner
-,r -.5,
c-ircuit, %e rosu~t-s Ln s a L,-, ra
o u t pu t t r ans f or-xa r an-~ 'z, a Ts.
jaustracter's note: ~V-ommp,ete
Card 1/1
Momlit, Janek;
The tako-off foot in athleteB. Acta chlr. orthap. trauma. Coch.
28 no.6;526-534 D 261.
2. Ortopedicke oddb:~eni Krajske detske nemocnice v Brne, prednosta
MIUDr. Jaromir Janek a chirargicki) odde-leni clcresni namocnice ve
Valticich, rednosta Mr. Jan Kralik.
IM physiol) (SPORT IEDIC11M)
CLDUROVA S V.
-------
Si!,,nificance of the filtering surface In a device for the transfu3ion
of blood and Its components. Probl. gamat. I perel. Krovi 8 no.9:
52-57 S 163. (MRA 17t9)
1. Iz laboratorii konservirovaniya krovi (zav. - prof. F.R.
Vinograd-Finkell) Mentrallmogo ordena Lenina instituta gematologii
I perelivaniya krovi (dlr. - dotsent A.Ya. Miselev) Mlnisterstvm
zdravookhraneniya SSSR.
USSR / Hvwan and Animal Physiology. Blood. T
Abs Jour: Ref Zhur-Biol., No go 1958, 41200.
Author : Pokrovskly, P. I.; Oldurova, S. V.
Inst : Not Given.
Title : The Effect of Prezerving Agents and the Duration
of Blood Sorage on the Survival of Erythrocytes
and Their Circulation Time In the Recipient.
Orig Pub: V sb.; Sovrem. probl gematol. I perelivanlya
krovi VYP- 32,k., Measiz, 1956, 164-173.
Abstract: An analysis of 121 transfusions of blood prepared
according to 7 formulas, stored for 5-15-25 days,
is presented. The number of donor erythrocytes ( E)
in &the recipient's blood was determined by the
Card 1/3
USSR / Hunan and Animal Physio-,,.;y, Blood. T
Abs Jour: Ref Zhur-Biol., No 19582 41200.
Abstract-, method of selective agglutination with anti-M and
anti-N sera by a method elaborated at the CIOHBTOL
(Central Institute of Hematology and Blood Trans-
fusion of the Order of Lenin). The erythrocytes
of the blood preverved with the formulae CIOHDTOL
No. 2.3.,6.,7,8,9, maintained the ability to survive
for a long period of time. The best media appear
to be solutions of glucose-eltrate (formula Do 7),
glucose saacharo-citrate (formula No 9), and gluc-
ose-citrate-saline (formula No 2); somewhat less
effective- saccharose-citrate solution (formula
?To 6); the erythrocytes of blood stored for 5 days
preserved with citrate with the addition of carbo-
hydrates had a survival time almost similar to that
of direct transfusions (86-89.7%). in transfusions
of blood stored for 15 days and preserved with
Card 2/3
49
USSR / Human and Animal Physiology. Blood. T
Abs Jour: Ref Zhur-Biol., No 9. 1958, 41200.
Abstract,: glucose-citrate and glucose-saccharose-citrate
media the survival time is 79-86%, 25 days -
67-73%. Erythrocytes of blood preserved for 5
days circulate In the recipient's blood for 11-14
weeks. E incapable of survival are broken down
mainly during the first days after transfusion,
particularly during the first 3 hours. This was
substantiated by the results of serum bilirubin
and Fe determinations. -- A. D. Beloborodova.
Card 3/3
OLDUROVA, S. 7. Cand Ued Soi -- (diss) of blood with *hv
now J47) preparation of the domestio
'blood BtAbIlizer natrog r'"dim
tribydroWlutarataj. Nos, 1957. 23 PP (Min of Health USSR. Cantkal Inst
for the Advanoed Training of Physicians), 2100 copies (XL, 42-57, 94)
:Bloc! pre3ervation vlt~., a new Russian stabilizer, acidic netrog
r-
L-ilth stirmOrY in 3religh) - ~rebl --emat.- t paral.krovi 2 no.4:
JI-Ar 057. (HURA 10: 10)
Montrz).1nogo o7dona leninn iWituta gemal-ologii I verell-
vaniya krovi (dlr. - deyatvitelln~7 ci,-,-en AFN 'o3SH -arof, A.A.
Ba--dovarw) MinintarDtva 2(1ravook'mra-,-rJ7,4 SSSR.
atabilizer t3cx11= salt of trloVglutnri~!
acia Oug))
mouo-subvIoltuted scdtim nrlt of trioxygInterte oacid as
3tabilizer In blood preserv. (RuB))
OLDUROVA, S.Y.
lxperimental and clinical
Russian blivd stabilizer,
70-7b ft 358
study of blood -preserved with a now
wId natroge Azerbamedgibur* no*32
(XnA 21:7)
11, Is laborstoril XonioarTiroyaniya krovi tsays prof, 7032 71nograd-
7inkell) TZentrallmogo ordena Lenins Inatituta Sematologil I perelivanl7a
krovi (dirktor - daystyltellmyy chlen AM SSSR prof. A.A. Bagdaisaro-Y).
(BWOD-40LIBCTION AND MISIMVITION)
(GIX.aIC ACID)
nNOGRA"IHM)3 7. R., prof.1 OLDUROVA, S. V.
Use of citric acid as a blood stabilizer In its prolonged preser-
vation. Probl. gemat. I perel. krovi no.20i43-45 163..
(MIRA 3J,.-:L2)
2. 1z TSentrallnogo ordena lenina institute gematologii I
pere2ivani7a krovi (dir. - deyBtvItel3nyy chlen AM SSSR prof. A. A.
Bagdasaroy [deceased)) Ministerstva zdravookbraneniya SSSR.
(BLOOD-COLIMTION AND PRESERVATION)
(CITRIC ACID)
CLDUROVA, S.V.
Experimental and climical BtUdy of the effectivemeBs of trans-
fuaions with blood preser7ed with citric acid imtead of acid
aodium citrate, Problogmat, I perelokrovi mo*3-1:52-55 161.
(MIRA 15:1)
1. 7z laboratorli konserviravani7a krovi (zav. - prof. F.R.
Vinograd-FimkeV) TSentralln o ordepa lanina iwtituta gem-
tologii i perelivani,. ra krovildir. - deyBtr.'tel3n.V chlem AIM
SSSR prof. A.A. Bagdasarvv Ideceassa] Ninioter3tva zdravookhraneni-ya
MR.
(BLOOD-TWISFUSION) (CITRIC ACID) (SODIUM CITHATE)
I r 0-
laborat~, r 1 kon~--., rov~ri krov i -~av
-,ere livan; v1" k-rov! (dir. dotsent. A.Ye. K..isolev) 'IlinisLerstva
t 03007-67
ACC NR. AP6033486 SOURCE CODE: URjD4l3/66jDo0/0l8jDD93/O093
3
INVENTOR: Vinograd-Finkel', 7. R.: Oldurova, S. V.
ORG3 none
TITLE3 Blood preservative,- Class 30, No. 186095
SOURCE: Izobret prom obraz tov zn, no. 18, 1966, 93
TOPIC TAGS3 preserved blood, trisodium sulfate, antibiotic, 'AY03PHO.'ejec
d 6 4D
ABSTRACT: An Author Certificate was issued for a blood preservative
containing sugars, antibiotics, citric acid, and water with phosphoric
acid salt (trisadium sulfate) added to extend the preservation periods
A variation of this preservative for preserving slightly diluted bloo,d
contains3 0,75 S citric acid, 3 g glucose, 0.75 g trisodium sulfate,
0.015 g levomycatin, and 100 nl double-di3tilled water. A vaTintion fo,r
preserving highly diluted blood contains: 3 g Citric acid, 15
levomycatin, and 1000 ml double-distilled water.
SUB CODBi 06/ SUB21 DATE: 26Jun64/
ATD PRESS: 5099
orig.:,Lrt. usi
00061
2~2
card
USSR/Medic~ne . Pancreatic Secretions Sep/Oct 52
"T~e Reaction of the Nerve Tissues on Pancreatic Se-
cretion," L. V. Oleandrov, Chair of Physiol, Moscow
Acad of Agric imeni K. A. Timiryazey
"Zhur Cbshe-n Biol" Vol 13, No 5., PP 336-345
"'Author discusses the historical argument bet the
school of 1. F. Favlov And the British physlol school
of Beilis and Starling on the causal mechanism regu-
latitig pancreatic secretions. After experimentation
on animals, author asserts his findings show this
238T49
mechanism as solely a neuro-humoral process (photo-
graphs.). Requests physiologists reading this article
to check his expts using methylene bluex treating it
as a microphysiol and micropharmacolmethod. Refers
to a boo% published by Bellis and Starling In 1902.
238T49
GREIDA, J020fj Xl=, VadIUSZj- OLMRCZYX, Andrzej
TeBticulaT sminoma vith pleural mestaBtaseB. Pol. przegl.
chir. 35 no.31iSupplmonti 1265-1269 14263
1. Z Ddd%AaIu Chimrgicznego (ordynators dr. JoGrends); 2
Wazialu Vewnetrznego 11 (ordyratml dr. Mies-)) S2pitala
Hiejskiego w Starachowicach. DyrektoT Szpitala: dre J.Grenda.
1, ~ DA J, ionor) ?'t '.LIICZLq.'p Andmaj
Px*c-cc&Lvv &Lr~!~Z -"m=cltat-l'cn, ',,?!ado Id-, le me Z13
. 13 !, , -65
M .4wil
lo "- Oddzialu V*drvxrlcmcCo Spplltala !,'o~ov,-.dejPgo
v 7:ioloaab OntimUrt dra =ode J, Clrman) a 2 3)nuau
AnootoziolDgil INIoromiki InIce ma, Ao oloa"BA)s
3UWK, X. OLIA ZTX, J.
N the properties of so called "thrombin prots"O. Act& pb.TmIvI.
polDn.3 ftrpl. 3: 16:1-1k4 1932. (OAL 2411)
2. Of the Iy4iituts of General and 3zp9rimental PAthology (Read-Pxof.
R. Kowarzyk, X.M. ) of Wroclaw Medical *JLcmAexy, 2. Thrombiij
-protease-is a preparation of fibrinol7sin with a very high titer,
containing besides fibrinolysiu thrombin in Tarying quantitilB,
MATKOWSU, Barbara; JANIAKOWA, AlInfil 012ARCZYK, Julian
Case of parahemophilia. Polski tygocl. Isk. 9 no.33:1050-1052
16 Aug 54.
2. 2 11 Xliuiki Chorob Yawnetrxnyeh A.M. we Vroclamiu, kiermmik-.
prof. ar Antoni 7alkiewicz i z III Zliniki Chordb Yownstrsnych A.M.
we Vroolavin, kierownik: prof. dr 34yard Siczeklik.
(MMRHAGIC DIATHISIS.
parabomophilia, caBs report)