SCIENTIFIC ABSTRACT GRECHKIN, N.P. - GRECHKO, M.K.

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• Collection: Scientific Abstracts
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• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: January 3, 2017
• Document Release Date: July 27, 2000
• Sequence Number: 14
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

USS?/Chemistr7 - Yhosphoric Acid 1947
. Cherdstry - S,-,-nthe�is
116:,rnthesis of Diphosphondialkyl Esters," B. A. Arbuzzov, Gorr Mlevl Acad Sci US.SR;
L4. 1. Grechkin, Chem Inst, Kazan Br, Acad Sci UIO-jii, 3 i-y
"Dok 'Nauk SSSR, Nova Ser" Vol LVII, Nlo
Givesdata collrcted during f~tudies on s-,Intheni- of dirlm3plhondialkyl ester:7, and,
I r, I-articular, triphosrhonalkyl esters usua.1 1y fout-A I v comp.-ards such n s R2 3r, F-C'112
or RSnHa13 witl-. coml-.lete ,-hof-,T--oric acid esters. Submitted, 14 N:nn- 19,17
F..'l 53TIS

ft compounds. It
jyl radicals at the 0
cork-^, LO==
IC A. Ailmmv att,l 1'. -01CV11kill JCIIVIU. 11114t., K.M.11
it ClIvill.) 20, 107 -Vtt 4j. 412148. -
milltiMet, (2.2% to.) aiml 41-7 it, Sle.Nil w4rinuil to )it'
violeuttly timix. tormp. 21,W) wul ykIdIrd 3.4 g.
in. 13J-41' (Ifour HIL011). Sitni-
Lilly. 6.4 x. HIPMEth With 10.8 9. HIioll plicheAled It,
1.101, 4.4%r 1.11 it. ilmol. cuhnlv~s all.
MP(OPO, (4-3 ;-) and 9.5 it. Bus,8111 at IsP
gavv 7-2`1 initil. PAMO&ItSpilla.). ill. :02-5' (de-
'UtIllm.). although %1111'~ Ltl w4s evolved. lIcAtiailt
Ph PO~ OMO Oita MCS) 30 utill. with 11,0 save Ito Cluntle.
I'llt IICI at t,min t,tnl,. yteld. :61"SIACI rapidly,
KUII in :1 hri. yuhis Me.SoOll, tit. 117 'W'.
I'll 1,41, Nle), it.) aml I! to. Mv,Sid, Saw.ifter.i vi.tirm
'Im"up. 29l 3,~
Sit
, utUity 7 jo. IiI.Sul.mid 0.5 it. Plit'(Wit),Afteir Preheat-
Ing to Mol, SAVe LLS a. Ff'SpIll'to)(OMPAJI. decompi.
2km~~kmt% whtl~ 4.5 it. mul 5 S. PhP(OP0i lpivt-.
at 1*;;,SvIP(U)(oPr)/1Aj,, dec"upS. 2,46 W.
All th-c prodircil at,- jij,N. Ito mg. olventIt; they mr
StAble it) 11,11 111(). Not upully .ICAVV III U.`;. [lei.
HIS110" Whole Ito- N.4011 VIC1.1. HjN.i I, Cl III
-
Aw vichk RtW.1, 'It Itwill IrIkill. Ilraltalit 11111,C1,
III,. In a -cal(A Iitl~ I-iW jtVC 30'", Ph,/,C: IIII, kits
%tvk)ll ill ill, pl-tuv 4 %tc,Nl'lk
I"S whil, 1-,tt)ll ot..~C 511~ 11h,11oN. 1.,.
IfeAting 7 K, Et.1mal and .1.9 S. 11h,11UHt to 1711' #,.vv
114111(o)SMEII. (Ict-oinpoo. 3116-8 " while the Vtoll.
Fiji) WaAlillits ji-tye 1.1 g. Ph,Etj'O. in. 121 -4'.
trise. 5.1 x. Nle..'iial and 4 ot. llh,llol-.t Save 9.S1 PA".
P(O)SxJfes, dvoitutig. :W-S", aml 1.73 g. llhjl~lllj.
wlii!c 4.6 it. F*111-Slit IIVA" With .1 g. I't4PU.%fC tU IjJIJ
gave Plit.11trPO, tit. 1141f-W. aml 4.2 jr. (91.51;) Et.801.
Meo4lis (11 S.) &)111 6.9 it. 1111'PoEt lu-Mcd to IW' X4'r
S. d,otiolog. 372-5% ukl 0.11 a
IIII?H110, While SA to. I-il'sill, .111,1 it S. 11110110Ht ii.m.
17.3'', h;l,NtIP(0WA,j.. J,%~,tup. .1.11 A% And 11h,-
m~ to lout 11,L). *title .,Fill
IV~ IICI ytelds I'lliPllill. in. M-4', &ud R,SfICI,, 41141
hot 01' ~ NaOll !Iititi[.Lrly gives IIIioP(),II and RSttU:
Cl almi Yields R'Sucl, and litt-Sunt-thly PII,POCI. fur 441.
treAtInclit ivillt Water gives 111ttPOIll: the actitut ,I A&I
tit it-flumeig Cillo I, %mitlar. a~ RISPiCli Aittl Plt,141,11 Are

Us=/chemistry - Cancerogenic Compounds Sep 52
"Synthesis of 3,4-Benzopyrene and 3,4,6,T-Dibenzo-
PYrene Derivatives Through Phenollone-9 and Benzan-
throne.." B. A. Arbuzov, N. P. Grechk-qn, Chem Inst
imeni A. Ye. Arbuzov, Kazan' Affiliate, Acad Sci
tt Zhur Obahch Khim" Vol 22, No 9, pp 1692-1-700
j
P
C%1 3,4,6j7-Dibenzopyrene and 1,2',3,4-naphtho-6,7-
crni be=opyrene both possess strong blastomogi-nic. ac-
tion; this prompted the synthesis of derivs of
3,4,6,7-dibenzopyrene. By treating benganthrone
,rith organomgnesiua coupds contg metbyl or methy
lene groups in the ortho position, the correspond-
ing 4-substituted benzanthrones were prepmred. Py-
rolysis of the latter yielded derivs of 3,4,6,7-di-
benzopyrene. In this manner, the following were
prepd. for the 1st time: 3-methyl-3,4,6.7-dibenzo-
pyre-ne., 1',3'-dimethyl-3,4,6,7-dibenzopyrene, 2'iso-
PrOPYl-3,4,6,7-dibenzopyrene, 31-methyl-41,5-ethy-
lene-3,4,6,7-dibenzopyrene) and 3,4,6,7-tribenzopy-
rene. In an analogous manner 3j,4-benzopyrene and
i-,21,3,4-naphthopyrene were prepd by starting with
phens,lone-q-through 1-substituted phenalones. The
high cancerogenic activity of 3,4,6,7-dibenzop~rrema
and the lack of activity in 21,3'-n&Phtho-314-
pyrene do not agree with the statemmt of A. Pull-
mn concerning the connection between cancerogenic
activity and the presence of a specific "K" field
in.the mol of the cancerogenic substance -Which
possesses an increased density of Pi electrong.
~c pt 4 1 no ~ 19 -. q q r3 '.rj)
212T34

- 'F~F
rl.:rlac w tile ;~flle4l~
14,
f lk_~tlllg PhSIf '.ith 0, (L-D
U~.r; gvlct similuirly at I'lo- 5"J'
1~!c ~4wv'_' %yuffir-A" thc follu'ving
of ~,nak isi f~:-ruicA: 79 5% (Afeo),P~O~-
'Vrjcl[j('lf'cl' b~., 111-150, I.29M, 1.4537; 651; ch-El;
esicr, bs 148., 1..4473; 72.5% di-Pr ctler. 1Z, Is)-,;
4*~ 1.12 7 7 ~9, 73% ditsc-llr estry, b, 1.10M) t
jis c~ler, b,.1 148.5-W" I ' 08,17*1
~4; 74"5
1.0701, 1.4-158,
I-B"
'o
id 152-3,64, 1.0552, 1.4495. Cf. U~Sq
A. 42404a. 0, M. Kosolajwl~
12 '~4 M C 4,3,

jSSR/Organic Chemistry - Synthetic Organic Chemistry, E-2
Abet Journalt Referat Zhur - IqUmiya, 11o 1, 1957, 956
Abstract: heated to 2100 with one mole (C2H5)2SnC'21 /Tc H ) P(0)2T2SII(C2H5)2
(DC) is obtained (MP 346-3490) together w14T'(W3pO' ~ehe forma-
tion of IX is appareDtly related to an intramoleculdr oxidation reac-
tion of VIII; this, however, is unestablished. The hydrolysio of IX
yields (C61102POH; the reaction is quantitative.
Card 2/2

GRUCHKIN, N.P,
Phosphororgante ethyle~nimine derivatives. Report no.l. Interaction of
ethylenimine with dialkylphosphoryl chlorides. Izv.AN SSSR.Otd.khim.nauk
no-5:538-543 Nr 156. (MLRA 9:9)
1.Xhimicheski7 institut imeni A.Ye.Arbuzova Kasanskogo filiala, AN SSSR.
(Phosphoryl chloride) (Ithylenimine)

GRECHKIN, N. F. (Chem. Inst. im. Acad. A. Ye. Arbuzov, Kazan Aff. AS U&4%)
"Phosphororganic Derivatives of Ethyle-aimine" (Fosfcrorganichesk-Ire proizvodn-yye
etilenimina)
Chemistry and Uses of Organophosphorcus Compounds
(Xhimiya i primeneniye fosfororganicheslzi-kh sr7jedneniy),
Trudy of First Conference, 8-10 December 1955, Kazan,
pp. Published by Kazan Affil. AS USSR, 1957
.2q3 -.V/7

dart-Aillris- Of
, A
"
at halogen derivatives of

id
lki
h
f
f di MT
.
i
UP V p
to, a
enam
et o
a
y
Nas ik 1957. l"I-S: cf.
C.A. St. Mo.- eating In seated tube 10 C. (E%O)tP(O)-
d 7.1 jr. PhCHiCI 4 hrs. at 13545" and 2 his,
at I&P pve 53% (EfQ)gp(O)N(CIfjPk)CA(iCJTjCJ. N.,
MAV. des 1.1621. nV 1.60M which Itydro(yu-I with MI
to phetrkliUMCITICI Ho tatt. tu. lot-26. Simitar
reuttau with 9.0 g. I-C4XCIfCt in 4 hts. at WS-&* pve
9.5 g. starting roaterials and 10 g, undistillable residue,
whkb an hydrof& with KCI gave I-CmIICfftNHCIftCl.-
HCI. m. 1964 . evidently the expected (FiO)tP(G)At-
(CHtCvjrt)ClrtCH.CicoWdzwtbedWd.atltnru. Trent-
Ing (if 6.6 C. 60 mi. MI. With
cam. amt. (2 C.) Cl in 60 Mi. CM it 06 and Sturiar tile
wae
r7t 1,4674-
M., wa,
tog.?
:WS LOA (RiOWO)XCjCMWjO hl SWid tUIj'46WjtI9 7.5
Y:
(tri 0 0) Cg,, 6 fict. f3a46
at
materfals-ud
POLO.
7V

4-1
ILI
S/02o/60/133/03/08/013
Bol 61BO68 82274
AUTHOR: Grechkin, N. P.
TITLE: Copolymerizatio of the Diethyleneamides of Phosphorus
AoidslWith Bifunctional Organic Compounds
PERIODICAL: Doklady Akademii nauk SSSR, 1960, Vol. 133) No- 3,
pp. 592 - 593
TEXT: In the introduction, the author refers to the N-phosphonium
aminoethylation of organic compounds described by him in an earlier
publication (Refs. 1-3)1 It was recently shown that the amides mentioned
in the title react according to the mentioned reaction involving a
cleavage of the two ethyleneimine rings. This induced the author to as
sume that the reaction mentioned in the title could lead to the forma-
tion of linear copolymers with phosphorus atoms in the chain (see
Scheme). The author deduced the alternate suboession-of the atoms from
the reaction of the monomer which had been studied earlier. The experi-
ments of the author showed that the amides in question can actually be
copolymerized with dicarboxylic acids, diamines, p-dichloromethyl aryls,
Card 1/3

Copolymerization of the Diethyleneamides of S1020V6011331031081013
Phosphorus Acids With Bifunctional Organic Bol 6/ 'D o68 82274
Compounds
and other bifunctional compounds. When equimolar amounts of diethylene-
amide of isopropyl thiophosphoric acid and sebacic acid are heated to
110 - 1200C, an exothermic reaction takes place which leads to the for-
mation of a rubber-like substance with a high elasticity coefficient,
In the course of a similar reaction, a solid transparent polymer having
the color of strong tea is formed by copolymerization of the diethylene-
amide of ethylphosphoric acid with benzidine (in molar ratios) and heat-
ing up to,125 - 1300C. This polymer (which was studied by means of a de-
vice designed by B. Ya. To-vtollbaum and M. P. Dianov) showed a state of
high elasticity between 150 Z-F-2200C Qig. 1). In th4 viscoun state,
filaments can be drawn from this polymer. Further experiments were car-
ried out by the author which lead to the formation of polymer substances
which are being studied at present. The capacity of the diethyleneamides
of the phosphorus acids to add to "the functional groups of organic com-
pounds can bd utilized.to prepare grafted and croselinked phosphorus-
containing pol4mere.AThey can be used to obtain croselinking"of:
1) polyamide. chains independently of the character of their end groups,
and 2) polyester chains with carboxyles as end groups. In a similar way,
Card 2/3

Copolymerization of the Diethyleneamides of, S/020/60/133/03/08/013
Phosphorus Acids With Bifunctional Organic B016/Bo68 82274
Compounds
the monoethyleneamides of phosphorus acids can be used for grafting
phosphonium groups to active end and aide groups of polymer molecules,
as was shown by relative experiments. Thus, a new method for the prepara-
tion of phosphorus-containing polymers by N-phosphonium aminoethylation
-was suggested by the author. There are 1 figure and 4 Soviet references.
ASSOCIATION: Khimicheskiy institut Kazanskogo filiala Akademii nauk SSSR
(Chemical Institute of the Kazan' Branch of the Academy of
Sciences, USS )
PRESENTED: March 7, 1960, by A. Ye. Arbuzov, Academician
SUBKITTED: March 4, 1960
Card 3/3

87165
3/062/60/000D/0 12/004/020
BOI 3/BO55
AUTHORS: qFLcjLkLn,_y'~...E. and Shagidullin, R. R.
TITLE: Organophosphorus Compounds of Ethylenimine Derivatives.
Communication III. Addition of Acids to 1~he Amides of
Phosphinic Acids With Ethylenimine
PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeloniye klilinicheskilch nauk,
1960, No. 12, pp. 2135-2139
TEXT: The present publication gives the results obtained in the N-diethyl-
phosphonaminoethylation (the term used by the authors) of carboxylic acids.
The authors apply this term to all reactions in which the amides of phos-
phinic acids with ethylenimine add to a number of compounds under cleavage
of the ethylenimine ring, as shown in Refs. 1 and 2. By this reaction, addi-
tion products of diethyl phosphinic acid ethyleneamide and several carboxylic
acids were obtained (Table). All the esters listed in the table were pre-
pared similarly: equimolar amounts of diethyl phosphinic acid ethyleneamide
and the acid were heated at 110-1200C in sealed tubes for 6-7 h. After dis-
tilling twice, the pure product separated. To establish the structure of the
Card 1/3

87165
Organophosphorus Compounds of Ethylenimine S10621601000101210041020
Derivatives. Communication III. Addition of B013/BO55
Acids to the Amides of Phosphinic Acids With
Ethylenimine
compounds obtained, the authors evaluated the infrared obsorption spectra
of the reaction products of diethylphosphinic acid ethyleneamide and acetic
respectively propionic acid. Diethyl phosphinic acid ethyl amide was used
as model substance. The spectra were run on a OKC-12 (IKS-12) spectrometer
with adjustable slit width using a NaCl prism in the 700-2400 cm-1 region
and a LiF prism in the 2300-36oo cm-1 region._The spectra of the three
above-mentioned compounds in the 2300-3600 cm 1 region are shown in Fig. 1:
1) (C 2H50)2 PNHC2H5 ; 2a) (C2H50)2 PNH-C H2 -CH2 OCOCH3or
11 1
0
2b) (C2H5 0)2PNN CH2-CH2 OH
11 CH
0 71- 3
0
3b) (C 2H50)2P-11 CH 2-CH 2-0H
CC11 CH
Card 2/3 A
3a) (C2 H50)2P -NH-CH 2-CH2-OCOCOH2 -CH3or
11
0

87165
Organophoaphoruij Compoundo of Ethylenimine Sc!/O 6 2 /60/0 0 0/0 12 / 00 4/0 2 0
Derivatives. Communication III. Addition of B013/BO55
Acids to the Amides of Phosphinic Acids With
Ethylenimine
The infrared spectra indicate the presence of intermolecular hydrogen bonds
between the nitrogen of the amide group and the oxygen atoms of the phos-
phone group (P=O) and the ether group (C-0). The structure of the substan-,,e
obtained by the wtion of diethyl phosphonic acid on diethyl phosphinic acid
ethylene amide is still unclear. The study is being continued. There are
1 figure, 1 table, and 6 references: 3 Soviet and 3 US.
ASSOCIATION: Khimicheskiy institut Kazanskogo filiala AN SSSR
(Chemical Institute of the Kazan' Branch of the AS USSR)
SUBMITTED: June 19, 1959
Card 3/3

SHAGIDULLIN, R.R., GRECHKINq M.P.
"Oscillatory spectra of certain diethylensamides of alkythiophosphoric acids.*
Kbimiya i Primuerilye Fos fort, rganic he-Hid. k h ")oymdIn-?iiY N-h-mniatn, a.a(I
avolication ol' organopho4nhorw-, contioury'5) A, YE,
~ubh by Kazar &M1. Ac-d, :~a!, 13'50it, 11~3cuw Q 'qo~
CollectIon of corw-,)It-tfi oap--r~* ore-iont.-d at tthf-~
Chemistry of rganoo~,aqphorum

8/058/63/COJ/001/056/120
A1601AI01
AIMIORS-. Shagidullin, R. R., Greahkin, N. P.
TIVY.: ~tfbratforrel spectra of some diethylene amides of
gikylthiophosphoric acids
PERIODICA~: ~eferk1ti'vhyy zkUk-n6l, Flzlka~ no. 1, 1963, 23, abstMat fbfi6
(In collection; "Khimiya I ;pri~n!enehiye tosToroMan..
M., AN SSSR, 1962, 112 - 115)
T M- The infrared absorption f3pectra and the Raman specti-A of A W&ek ot
new diethlene amides of alkyl-thlophosphoric acids were ihveatigatddi. ti is shd~ft
that the pulsation vibrations of the eihylenimine ring in the Vr6sbfihe ot Oios-
phorus appear to be adequately characteristic by their frequency and Intensit~,
and that the corresponding lines artA bands, which clearly appear in the infrared
spectra, may servo as a good analytic Indication. th Vie region of 41(0 am is
vibrationn of the C - N bonds at the ring are_ T"' footed, A strong Infrarvd ab-
sorl)tion was obseried in the region of 930 cm . it Is identified with an asynt.-
OdH 1/2

Vibrational spectra of;.;
Metric vibration of the Hhg ~ z I
[Abstracter's note: compic4:6 ti~dfiijgii&)
-9/058/63/000/00 W056/10
A160/Aloi
Yu. ftxurenko . y
Card 2/2

GRECHKIN, N.P.i NURETDINOV, I.A.
Reactions of ethyleneamides of phosphorus acids with some
unsaturated acids and all3damine. Izv. AN SSSR Otd.khim.
nauk no.2.,295-298 F 162. (MIRA 15.-2)
1. Khimicheskiy institut im. A.Ye.Arbuzova Kazanokogo filiala
AN SSSR i Institut organi-2heakoy khimii AN SSSR, Kazan'.
Phosphoric acid)
Msaturated compounds)

GRECHKIN., N.F.
Organophosphorus derivatives of azetidJne. Izv.All SSSR.Otd.khi;-a-
nauk no.8:1495 Ag 162. OMU 15:8)
1. Khimicheskiy institut im. A.Ye.Arbuzova AN SSSR.
(Phosphorus organic compounds) (Azetidine)

----WCHKIN N.P..- GRISHINA, L.N.
1 .1
Ethylene amides of g1rcolphomphorous acids. Dokle AN SSSR 146
no.6:1333-1334 0 162. (MBA 15 -- 10)
I* Mimicheskiy institui im. A.Ye. Arbuzova AN SSSR. PredBtavleno
almdemikom A.Ye.h-buzovym.
(Phosphorous acid) (Rearrangements (Chemistry))

GRECHKIN, N.P.; NURETDINCV, I.A.
Organophosphoric derivatives of othyleneimine. Report NO-5:
Mono- and polyfunctional monomers. Izv.AN SSSR.Otd.khim.nauk
no.2002-306 F 163. (MIRA 16:4)
1. Khimich*kiy institut im. A.Ye.Arbuzova i Institut organicheskoy
khimii AN S~SR, Kazan'.
(Ethylene compounds)
(Phosphorus organic compounds)

NURETDINOVp I.A.; GRECHKINP N.P.
Synthesis of some triamides of phosphorus acids. Izv. AN SSBR.
Ser. khim. no.lDil883-1885 0 064. (MIRA M12)
1. Institut organicheokoy khim-li AN SSSR, Kazan'.

GREC.-HKIDIP N.P.; GRIS11171A, L.N.
Propertiva of othylenard0no of' glycolpbofsphrzoun fin-Ilds. Tzv.
AN SSSR Ser. k1jim. no.M.15W-115104 165. (MIRA 18,.9)
1. Khirritcheskly institut im. A.Ye. Arbuzova AN SSSR.

GRECHKINJ,-N.P.; SHAGIDULLIN, R.R.; GRISHINA, L.N.
Structure of the product of reaction between phosphite and
ethanolamine. Dokl. AN SSSR 161 no.1:115-117 Mr 165.
(MIRA 18:3)
1. Khimicheskiy institut im. A.Ye. Arbuzova All SSSR, Kazan'.
Submitted July 31, 1964.

fil"thylerilm.1de-s of Ollie-vj- and -,V
All,, SSSR, Ser. khim.
'an-c'neokuy k!'AnA." All
In3titut org
institut imeni ltrbuyuva ~.Il

. GRECH,K.IN,-N,.P.; KHAMITOV, R.N.
Organophosphorus derivatives of azatidine. Phosphoric acid azetidides.
Dokl. AN SSSR 162 no.5:1063-1064 Je 165. (KRA 18s7)
1. Xhimicheskiy institut im. A.Ye. Arbuzova AN SSSR.Submitted
December 7, 1961+. -

L 26*JL-��_ EWTWAvvPu) RIK
ACC NR, AP017)65 SOURCE GODEj UR/OO62/65/QO0/OO8/102/1304
AUTHOR: Grechkin. N. P.; Qriehina, L. N.
ORG: Chemical Institute im. A, Y66 Arbuzov, AN SSSR.(Udmicheskiy institut AN SSSR),
TITLE: Properties of.ethyleneamides of glycolphosphorous acids
SOURCE: AN SSSR. Izvestiya. Seriya khimicheskaya, no. 8, 1965, i502-1504

TOPIC TAGS: organic amide-, o
rganic phosphorus compound, organic imine compound)
.acetic acid
.ABSTRACT: The reactions of glyeolphosphorous acids with organic

.compounds possessing a-labile hydrogen atom were studied,
in an
,attempt to.open the ethyleneimine ring in the amides of certain
'glyoolphdaphorous acids with various aminest in all oases a trane-~"
amirihtion teaotions liberation of free ethyleneimine and formation
of a new ailde of-glyeolphosphorous acid - was observedg lndicat-.--:~'
.ing extremely low strength of the nitrogen-phosphorus bond. The
yields-of the now amides produced in transamination are,low, evi-
'

.
.
!dently.au a result of simultaneous ammonolyals of the aliphatic
A
'Wheri the ethyleneamidee of glyeolphosphoroua acids are
treated with acetic acid, they are deaminatedp forming.the ethylenedi
amide of aoetid . acid and the f ree qt.hyllene. glyoolphoop4orous ~ aolde 0
-
the lAter
in rather high yields (664%). Orig. art. has: 2 tables.
SUB CODE: 07 SUBK DATE., :18Dec64 ORIG REF 004 / OTH MW: 001
UDC: 542&91461i718.1'
Card 1/11'~'

L 06529-67 EWT(m) rdp(j) RM
46C--
ACC NR. APTOW
'NURMINOV, I. A., 6KAGIUILLIN, R. R., Sim]
Institute of Organic mintry, Aondemy o f
.3on z COD;,.,:U 006'7
Yu- Ya.) GrMHM N. P-P
0-0-M-11) AZAD' (Indtl"Uut
UN
"Amides of Phenylvinylphosphinic Acid"
Moscow, Izvestiya Aks4emii Nauk SSSR, Seriya Khimicheskaya, No 5, 1966, PP 839-
Abstract: AmIdes of phenylvinylphosphinic acid were produced by reaction of
the acid with the (witne. The ethyloneimide of plianyl-beta-cliloi~oetllvlpl)ooptlinic
acid was produced by reaction of phenyl-beta-chloroethylphosphinic acid chloride
with ethyleneimine in the presence of triethylamine as a hydrogen chloride
pLeceptor, in an unsuccessful attempt to produce the ethyleneimide of phenyl-
beta-ethyleneiminoethylphor.phinic acid. The infrared spectra of the substances
obtained were studiqd. The presence of ppi-dpi conjugation in the systems con-
sidered was hypothesi*ed on the basis of the frequencies of the F=O and C--C
groups. The rate of inversion of nitrogen in ethyleneimides of phenylvinyl-
phosphinic and phepyl-beta-chloroethylph9op4nic acids is very high acq rding;
~qAke_proton.maxaetic resonance_data. Orig. art. has: 2 figures and 2 tables.
IC TAGS: organic amide, vinyl compound, phosphinic acid
CODE: 07-/ SUBIT DATE: 28 Dec 63 / ORIG REF: 004 / OTH RCF: 003
Card l/ -4 UDC: 543.422:542.951.1:661.718.1

ACC NR, AP701072; ODS: UR/0062/66/000/008/1466/1467
SOURCE C
AUT;IOR: Nitrotdinov, 1. A.; Grechkinj M. P.
ORG: in!;titute of Organic and -c,hysical Chemistryv Academy of Sciences
USSR (Institut organicheskoy I fizichaskoy Ichimli AN SSSR)
1 U': int-araction of monoethyleni-mides of acids of -,entavalenc
phos;)horu5 with thioacetic acid
SOURCE: AN SSSR. IZVestlya. Serlya, khImicheskaya, no. 8, 1966, 1466-1467
I'M11C TA(74'#I M bpocitrujit, ortfsifild phoupikorkill 0(impoiIIIII, oompowil
Sm3 coi)-':': 07 :
A10-TiUM: N-phoaphorylated 0-ace tyliiwircaptoathyl timl tic, 6 vvjrv propbrod by ro-letion
of rionoethylenimides of acids of pentavalent phosphorus with thioacetic acid. The
reaction proceeded readily without a catalyst, upon heating on a boiling water
bath; sufficiently pure products were obtained in good yields, generally 75% or
above. Seven new derivatives were prepared and characterized. Their structures
were confimed b.Y their infrared spectra. Orig. art. has: I formula and I table.
LJPIRS: 40,3517
Card 1/1
UDC:.- 542.951.1 + 546.185 + 1~,7,
:,229

ACC NRt AP7011831 SOURCE CODES uR/0079/66/036/010/1862/1862
AUTHOR: Grachkin, N. P. IMMItov, a. N.
ORG: none
TITLZt New method of producing osetidides of dialkylphosphoric acids
SOURCE: Zhurnal obshchey khInti, v. 36, no. 10, 19MO 1862
TOPIC TAGS: chemistry technique, phosphoric acid, szetitide
SUB CODE: 07
ABSTRAM Azetidine reacts readily with dialkylphosphites and carbon tetrachloride,
-to form azetidides of dialkylphosphoric acids. Azet1dides of diethylphosphorico
di-n-propylphosphorle, and di-n-butylphosphoric acids were prepared in 77 to 850
yields by conducting the reaction In other solution at temperatures from -50 to i5p-~
Their properties were 1dentleal with those prepared from the acid cblorides and
by transamidation. The imthod Is said to be covivenlent and gives bigh yields.
f7raat 40,
Card UDCi 547.261118

y f"M T11- I lp .1, MN
k N.M., 7-AW-ROVErY, FILT OVT.Cp.,. F, *~. T' ,
P.P,pJ.d oxf--.ution !-~f dwia-lopment wol-kings at the No. 1/,~ Tallne
Of the :-~~51,hp2llnugoll combine. Ugoll 40 no.8,20-2-2 I g 16.C
,I*
(MIMP 18;8)

-.GRICHKINO N.Z. (Yenlesyek).
Problem from thepages of the Polish journal "Vatematika" an methods
of teaching algebra..Mat. v shkole no.6:78-82 N-D '58.
(MIRA 11:12)
(Poland-Algebra-Study and teaching)

GRECHKIN, N.Z, (Yoninernk)
, j
Study of elementary accounting, In schoola of tho Pollob Poople'a
Repilblic. Hat. v shkole no.2:74-76 Mr-Ap '59.
(141RA 12:6)
(PolanA-kccounting-Study and teaching)

YELOISKA. Lyadvika (Jelenska, Ladwikel. Prinimal uchastiye RUSETSKIY.
AONO; Nz jtransiatorl; MOLCHANOV, M.P., red.;
MAMOVA, N.N., takhn.red.
[Methodology of t69 teaching of arithmetic and Peometry in
g
elementary schools: teachers manual] Netodika arifmatiki i
geometrii v pervye gody obuchenita; posobis dlia uchitelei
nachallnoi shkoly. Moskva. Goo.uchebno-pedagog.i7d-vo M-va
proev.RSFSR, 1960. 175 p. Translated from the Polish.
(MIRA 13:11)
(Mathematics--Study and teaching)

1. GRECHIl.'IN, P. 3.
2. US31? WO)
4. Conveying Machinery
7. Hand truck for the apiary, Pchelovodstvo 30 no. 3, 1953.
9. Monthl List of Russian Accessions, Library of Congress, APRIL 1953, Uncl.

ACCESSION XR: AP3005630 S/W46/63/009/003/0379/0381
AUTHORS: G_xWo!~! ~,V. Nosdrev, V. -F.
TITLZ-. Ultrasound velocity in the critical region of the ternary system benzene-
methanol-toluene
SOURCE: Akusticheskiy zhurnalq v. 9. no. 3. 19631 379-381
TOPIC TAGS: ternary system., benzene-mthanol-toluene system., benzenep methanol,
toluene, ultrasound, acoustics, ultrasound velocity, ternary systems acoustics,
critical region
ABSTRACT: The velocity of ultrasound propagation in ternary liquids was studied in
order to provide data missing in the literature, The liquids used in this investi-
gation consisted of the previously studied binary benzene-methanol mixtures (V. F,
Nozdrev, G. D. Tarantova* Skorost' zvuka v sistema benzol-mitilovy*y spirt v
kritichaskoy oblasti. kkust. sh., 1961, 7s 4,, 496-497) diluted with various amounts
of toluene. The velocity of the ultrasonic wave propagation was determined optical-
ly. Z-Abstracter's note: hereafter the determinations are referred to by the
authors as "acoustice"JIn the critical range the behavior of the mixtures was
c,rd 1/4

ACCMIOX NR-. Ap3oo563o
found to be analogous to the behavior of their separate components, Throughout the
entire range of temperatures tested the ultrasound propagation velocities in the
liquid phase exceeded the velocities in the saturated vapors. In both media the
velocities decreased sharply near the critical point and increajed' rapidly beyond
this point. The minimal velocities at the critical points were measured with a
fair degree of accuracy. Using the data on the 4ensities of the ternary mixture
and on the ultrasound propagation velocities, the authors have calculated the co-
efficients of adiabatic compressibility for some of these mixturese ngure 1 of
the Enclosure shows the relation of these coefficientsA8 s) to the temperatures and
the compositions. The coefficients p for the ternary mixtures were found to ex-
~ jfi~
ceed those for the separate components and for the binary mixtures. The acoustical
method-of investigation provided other data useful in practical and theoretical
studieu dealing with the physicochemical properties of complex mixtures. As an
example, the authors present a table showing critical temperatures and pressures
for all. the mixtures investigated in this work. Orig. art. hast 2 graphs and 1
table.
ASSOCIATION: Moskovskiy ablastnoy pedagogicheskiy institut im. N. K. Krupskoy
(HosevOistrict Teachers Institute)
Card

ACCESSION NR: Ap3oo563o
. SUBMITTED: 08APr63 '
STB GODEs PH
I
I
I
. . t
- A I
DATZ AOQs 27Aug63
NO W 50Vs 003
I
ENCL: ~--'
OTH.71t: 000
co,d 3/4

-.ACCESSIoN n: AP3W5630
s S;Ie, at-'
i
s
03
0 41,
J5 at
Fig. 1
car,d 4/4
ENCLOSURE: 01
IU. 1e Relation of the coefficient of
compressibility to the mixture temperature and
camposition. The curves correspond to: 1) 40% of
Y6 in CH 30H$- 2) 16.7% of Y6 in CH 3) CH 39H'.
4 20% of C7H8 in the mixture containing 20% of
%Ffo in CH3 OH; 5) 80% of CP8 ~n the xixtur~
containing 40% of Cd6 in CH?0
ta

NOUREV, V.F.; =a-"N -VI-1.
Deterrination of the critical curves of ternary mixtures by the
ultra-ac)ustic method. Zhur.fiz.1chim- 38 no.11:2663-2664 N 164.
(MIRA 18:2)
1. Moskovskiy oblastnoy pedagogicheskiy institut.

!"i, V. P.
20916 Grechkin, V. P. Uzkotelyye elatki, povrezhdayushehlye osinu, i mery
bor'by s nimi. V sb: Tssledovaniya po les. khoz-vu. Y, - L., 1949, s. 25i-64, -
Bibliogr: 17 nazu.
SO: LEMPIS ZHIT-NAL STATEY - Vol. 28, Moskva, 1949

GRXGHKIN, V~P.,- BUUOBY14, A.N., naucNiyy red.: KOGAN, H*I., prof., vadushchiy
[Studios .on the biology of forest postal Ocherki po biolo'gii vredite-
loi leen, Moskva, lzd-vo Hook. ob-.va ispytatelei prirody, 1951. 149 p.
(H~terialy k poznanHu fauny i flory.SSSR. Otdel zoologicheskii
(Kim it
no.31). 1:3)
(Forest insects)

1. GRECHKIN, V.P.
2. USSR (600)
7. "Bacterial Canker of Poplars and the Part Played by Insects In its Spread",
Lesnoye Khozyaystvo, No 6, 1951, pp 69-71.
9. Mikrobiolo&Lla, Vol XXI, Issue 1, Moscow, Jan-Feb 1952, pp 121-132. Unclassified

USSR / General and Specialized Zoology. Insects. P
Abs Jour: Ref Zhur-Biol., No 2j 1958, 6817.
Author
Inst : AS Tadzhik SSR.
Title : Cicades as Pests of Mountain Forest Cultures of
Central Asia.
Orig Pub: Dokl. AN TadzhSSR, 1956, No 18, 51-60.
Abstract: The emergence of the big white winged 01 'cade
(Paharia zevara) continues from May 20th up to
July. The female make cuts up to 8ma in length
in branches and small trunkd 0.3-2 cm in width.
The cuts are divided into two, situated one above
another cavities in the wood; into each cavity
the insects deposit 20-34 eggs. The larvae emerge
in the middle of August, dig into the soil and
feed on the juice of roots, mostly bf-bushes.
Card 1/3

USSR / General and 0-pecialized Zoology. Insects.
Abs Jour: Ref Zhur-Biol., No 2, 1958, 6817.
Abstract: Generation takes place, possibly once, within more
than 4-5 years. The wing-variegated cicades (Cic-
adatra querula) develop in the same way. The fe-
males make cuts 5 mm. in length on the stems of
herbaceous plants, on the thick petioles of the
trees' leaves, on branches and small trunkd 1.5-8
mm in width; 10-16 eggs are deposited into each
out. The females deposit their eggs in the forest
on special varieties of trees, in the plantings
indiscriminately on all trees. The larvae feed
on the roots of herbaceous plants. These cicades
have not more than one generation in 4 years.
Thousands of this cicade variety inhabit separate
branches and bushes, while of the white4winged
cicada there are only a few dozen. The growth of
the trees and bushes is checked by the damage of
Card 2/3
27

USSR / General and Specialized Zoology. Insects. P
Abs Jour: Ruf Zhur-111.ol.o No P,, 1956, U317.
Abstract: the white winged oicade; branches and little
trunks become ourved, sometime they become thicker,
dry out and break. The cuts open, forming wounds
5-10 cm in length. The damage to plantings by
both varieties of cicades consisted mostly in
growth checking. The chief methods of controlling
the cicades were agrotechnical. -- A. P. Adrianov.
Card 3/3

GRECHKI N, V. P.
Some principal representatives of %he Ingect post fanna In the
mountain forests of UJIMatkni (with linglish summary in insert].
Zool.shur. 35 no.10:1476-1493 0 1560' (MLRA 10:1)
1. 5wra Moskovskays aerofoto1*s6ustro1tel'nRT& skepeditsiya.
(TaJitt6tan-yerest insects)

tMACHKIN, TY.', inzh. ; ZHOKHOV, P.. inzh.
-
larch spinner, a dangerous past of conifer forests. Mu~m i Pered.
op.v sellkhoz. 9 n0-7:45-47 J1 '59. (MIW, 12:11)
(Coniferao-Diseases and posts)

DREMICHEV, I.D.; GRECHKIN, V.P.; KUROCHKIN' T.D., red.; SAVIN, B.V.,
red.-leksikograf-, VE-OVSKAYA, N.A., tekhn.red.
(Nnglish-Ruasian dictionary of rocket weapons] Anglo-rueskii
slovarl po reaktivnomu oruzhiiu. Moskva, Voen.izd-vo H-va obor.
sssR. 196o. 383 P. (MIRA 13:12)
(Rockets (Ordnance)--Dictionaries)
(English languags--Dictionaries--Russian)

GRECHKIN. Y.P.
Siberian silkwOrS (Dendrolimus sibiricus Tschetw.) as a forest
post in Mongolia. Zool-thur- 39 no.i:84-96 Ja 160.
(MRk 13:5)
1. 5th Moscow Air-Photo forest Management Expedition.
(Hougolia-Moths) (larch-4DIseases and pests)

GqFPCHFIN, V, P
Anglo-Russkiy siovart po re-~Vtlvriomu oruz~Ayu- Sost.
'C.D. Dremichev W 'I.'. Grechkin. Moskva, Vaye~:iz~lnt,
IcAo.
3'3 P. tables.
"Ukavit,~,I' Russkikh terminov" p. 766-380.

ZHOYJIOV, Pavel Ivenovich; GREG !L o KOLOMIYETS,
HKIN, Vladim: _E~~
Nikolay Grigoorlyee J -VYSVI'.SfUUA, A.Leksandra Vladimirovna;
UNSHCHANOV, Sergey Stepanovich; VOROIITSOV, A.I.,, red.;
,FUXSv Ye.A.v red.izd-va; PAIIAKHINA, N.P.,, tekhn. red.
(Tent caterpillar, Dendrolimus siboricuss and measures for
its control] Sibirskii shelkopriad i mery bor'by s nim. Pod
obshchei red. N.G.Kolcmiitsa i P.I.Zhokhova. Moskva, Gos-
lesbumizdat,, 1961. 139 p. (MIRA 15:4)
(Tent caterpillars)

GRECHKIN. V.P.
Large bark beetle,Ips.subelongatus Motsch. Zool. zhur. 41
no.4:552-559 Ap '62. (MIRA 15:4)
1. Fifth Moscow Air-Photo-Foreat Manageing Expedition.
(Bark beetles)

GRECHKRI, Vladimir I'allovJch; VOR'ONTSOV, Alek-sey Jvarw;ich
(Pests and diseases of poplars and the measures for their
control.] Vrediteli i bolezai topolei i mer-j bor'by s n1mi.
Moskva, Goslesbumizdat, 1962. 148 p. (MIRA 19:1)

i 17
EPF(~)/EPR/EPA($)-2hw(j)/EWT(M)/T PC~Orw4#34/pt-10 W. x.,
AT6002136 - '.06000/64/000/000/0267/0272
ACCM10b( 14fi:-
ATMORi Kalabtna A V I
Grochkin Ye Fs: BYchkqv%_ TO.; r1HWovq,_A.
N. A
Tyukavkina, a =r~ ~i6v_F' 5EH
Synthesis of some now 1- others of their conversion
Ind
SOMCES 'inteza
michaskogo a sintez I ovoyetva monor
-Aeftew
(The synthesis and prope Uear it in6 _'_rrA_V0 Naukas 1964, 267-272
r nomers . oscowt
TOPIC TAGS: vinyl aryl ether aromatic other, phenol derivative, diphenylpro A'.
derivative# diphonolpropane divi er, polyether synthesits, boron trifluorlde
RY
TRA
JM CT: Studies on the synthesis of vinylaryl ethers were expanded by the prepara
tion of new ethers from substituted phenols and of their conversion products to obtain
highly reactive and readily polymerizing compounds. The compouads reacted to prepaft,,i
vinylaryl ethers included nitro-, Wow-, bromo-, chloronitro-, andUtophenols -and
p, p-dihydror4diphenylpropano; the r tioll products were purified by steam distillation
or recrystallization. p1bMerizationt as mainly atudied with diphenolpropane divinyl
other. Its hamopolymer, obtained atm with boron trifluorlde, oontains an inzoluble
fraction of onselinked polymer; ft copolymortzeHon. with larp amounts of VtnY1j*oDY1;:-
ether imprwTo ths thermal stability.of the product markedly an compared with-V Wl-,
cc
rd 1/2

L 22650-~O

CESSION NR: AT6003136
A
CI
homopolyme.r. Routes for -produoft di-. and triddoroothYl-o and 0-,Chloroak
phenyl ether
and J3 J3-di6hl6ro- vinyl-aryl ethers are established. The reactions of vinylax7l ethers
with i;hosphorus prdduce estets and &old chlorides ofl-aryloxy"l-
phosphonic and thiophosphonlo acids, PolMerization of
-combasoble I at 350 0.
gives anon whtch does not melt Orig. art, has: I

orn Isla
f and 3 tables.,

ASSOCIATION: None
~
4 ,

,.,
66".
"".~,
- CaDst"-C16
'-,'EK0L GO
30i~i6i*'~-,."
SUBMrrrEDI~
.
.
.
.
-
i*,(,7
O~~ 2
-40 REP 50V1 013 ......

2/2
Card

GRECHKINA, A. K.
"Causes of Nontrau:natic Death of Children." Dr Med Sci., Kiev Order of
Labor Red Banner Medical Inst Imeni Academician A. A. Bogomolets, Ministry of
Health USSR, Kiev, 1954. (KL, No 5, Jan 55)
Survey of Scientific and Technical Dissertations Defended at USSR Higher
Educational Institutions (12)
SO: Sum. No. 556, 24 Jun 55

POLIKARPOCHKINy V.V.j KOROTAYEVA, I.Ya.;_qM~I~INA, Ye.A.; GAFONTSEV, G.P,
Rilatiofishi~-betw6en the liquid and solid phasp-s of stray flux.
Geokhimiia no.2:198-210 F 165. (NTRA 18:6)
1. Institut geokhimii Sibirskogo otdeleniya AN.SSSR,, Irkutsk.

YEDIAKOV, Konstantin Semenovich; TARAMNKO~ Nikolay Vasillyevich;
LUTOV, Viktor Mikhaylovich; GRECHKIVSKIY,, V S P inzh., red.;
RMAN1,11KOVII F., red.; KARWAVIIIA, 1e-.,--te-k-h-n-.--r--e-&.-
(Vow methods for chip breaking] Novoe v struzbkolomanii. Li-
potsk, Lipetskoe knizhnoe izd-vo, 1960. 35 p ~MIPA 15:3)
(Metal cutting)

GRECHKO, A., (g.Druzhkovka, Stalinskoy oblasti); KULIKOV, I., inzh.-konfitruktor
(g Druzhkov)-A, Stalinskoy oblasti)
Maebine tools desIgnod by operator Persianov. Izobr.i rats. no-12:37
D 158. (141RA 11:12)
1. Nacballnik paroollovogo teekha Toretskogo masbinostroltellnogo
zavoda (for Grechko). 2. Toretskiy manhinostroitellnyy 2avod (for
Kulikov).
(macidn" tools)

ACC NR- It 1: 7 0 0 t) 0 08 SOURCE CODE: UR/900 3-/67/000 /-0-4-6/0001-/000"1
AUTHOR: Grechko, A. (Marshal of Soviet Union)
OR G none
TITLE: CAarshal A. Grechko on the Soviet Armed Forc
SOURCE: Izvestiya, no. h6, 23 Feb 67, p. 1, col. 1-4. p. 2, col. 1-7
.TOPIC TAGS: military policy, military status
ABSTRACT: 1,Urshal Grechko writes that the Soviet Armed Forces have everything for
the reliable defense of the country. As regards the small new solid-fuel.
rockets on mobile launchers, they are virtually undetectable by air and
~space reconnaissance and are capable of destroying targets at great
distances. There is no region in the ocean where the Soviet submarine
rocket fleet could not function. The Soviet might does not reside only
in such equipment and new weapons. There is no intention, of course, to
minimize the significance of such means as do those who consider nuclear
weapons as a paper tiger. To take such a viewpoint is to subject the
defense of peace to the gravest danger. The Soviet military science is
based on the fact that the outcome of war will not be decided by
equipment alone, but also by the people who are armed with it. [NC]
SUB CODE: ' 15 /* SUB'M DATE' "none ATD PRESS: 5.1.15
Card UDC:none

ACC NR: A-,; -1 0 06 0 0 8 SOURCE CODE: UR/9003/67/ooo/o46/0001/0001
AUTHOR: Grechko, A. (Marshal of Soviet Union)
ORG: none
,A,,, 4 0, f. L.-
earshal A. Grechko on the Soviet Arm
TITLE. ed ForceD
SOURCE: Izvestiya, no. h6, 23 Feb 67, P. 1, col. 1-4, p. 2, col. 1-7
.TOPIC TAGS: military policSr, military status
ABSTRACT:
SUB CODE;
Card
Kirshal Grechko writes that the Soviet krmed Forces have everything for
the reliable defense of the country. As regards the small new solid-fuel.
rockets on mobile launchers, they are virtually undetectable by air and
-space reconnaissance and are capable of destroying targets at great
.distances. There is no region in the ocean where the Soviet submarine
rocket fleet could not function. The Soviet might does not reside only
in such equipment and new weapons. There is no intention, of course, to
minimize the significance of such means as do those who consider nuclear
'Weapons as a paper tiger. To take such a viewpoint is to subject the L
defense of peace to the gravest danger. The Soviet military science is
based on the fact that the outcome of war will not be decided by
.equipment alone, but also by the people who are armed with it. [NCJ
15/ SUBM DATE: none/ ATD PRESS: 5115
UDC:none

GUGHKO, A.A.
-
Efficiency in the Novoufa oil refinery. Neftianik 1 no.11:19-20
N 156. (NLRA 9:12)
1. Inzhaner po izobretatelletvu Novoufimakogo neftepererabatyva-
ushchego savoda.
(Novoufa-Patrojeum-Refining)

GRECHKO, A.A.
Improvement in desien at the enlarged pressure-vaciam distillation
plant. Dokl.AN Arm.SSR 24 no,2:23-25 157. (KRA 10:4)
I.Inshener po izobretatelletvu Movoufteskogo neftepprorabatyvarushchogo
zavoda.
(Ufa-Petrolemm-Refining)

GRECHKO, A.A.# mar Sovetakogo Soyuza.
Irl
On guard over the Soviet homelarml. Voen. nr-n. 37 no. 2:1-2
F 161. (MIRA 14:1)
(Russia-Armed foroes)
it

ACC NRI AT5022181 SOURCE, CODE: UR/0000/65/000/000/000~3/0020---'---
AUTHOR:, Qrechko, A. A.. (Marshal of the Soviet Union, Commander-in-chief of the
joint armed forces of the countries of the Warsaw:.Pact)
ORG: Joint Armed Forces of the Countries of the Warsaw Pact (Oblyedinennyye
vooruzhennyye sily stran Varshavskogo Dogovora)
TITLE: The military alliance of fraternal peoples
SOURCE: V yedinom stroyu (In a united system). Moscow, Voyenizdat M-va Obor. SSSR,
1965, 3-20
TOPIC TAGS: armed force organization, military personnel, political history, political
personnel
ABSTRACT: The author discusses the origin and development of the armed forces of the
countries of the Warsaw Pact. After World War 11 the ruling circles in the West, headed by
the USA, became alarmed at the growing revolutionary movement of the people and adopted
a reactionary stand In foreign policy, ekemplified by the policies of "cold war" and 11fron.
position of strength." The beginnings i6re laid by Churchill in his Fulton speech, and the
practical results were the Truman Doctrine, the Marshall Plan, and NATO, SEATO, and
CENTO. US military bases were built on the territories of many countries with the aim of
attacking the socialist countries. American troops occupied the Chinese island of Taiwan, and
the USA launched an aggressive war againBt the Korean people. The impeyialists split up
Card 1/2

L _8~26 - 66
ACC NR: AX5022181
Germany and organized the revenge-seeking West German state which started hastily rebuilding
Its war potential. West Germany became a member of the aggressive NATO block, as a re-
sult of which the peace-loving countries of Europe grouped together into a defense pact which
was signed in Warsaw. The aggressive policies of the NATO block and the defensive role of
the Warsaw Pact countries are discussed. The composition, strength, and aims of the entire
socialist camp are presented. This includes 14 countries with 25% of the territory, 35% of
the population, and 38% of the industrial output of the world. Recent aggressive acts of US
imperialists include the attempt to strangle the liberation struggle of the people of South
Vietnam, expansion of military intervention in Laos, and direct aggression against the
Democratic Republic of Vietnam, which Is the advance post of the socialist camp in Southeast
Asia. Brief historical sketches of countries of the Warsaw Pact are given. The assistance
extended by the Soviet Union to the cause of socialism is noted, including the active aid given
to the revolutionary struggle in China in the 1920's, Soviet volunteers piloting aircraft to-
gether with their Chinese brothers against the Japanese, and the liberation of many lands in
World War H. The role of other countries in these struggles is noted. Orig. art. has:
1 figure.
SUB CODE: MS, GO / SUBM DATE: 15Apr65
jW

ZHUKOT, N.;
Help for the lagging ic the law of competition. Mast. ugl. 7 n0.1:
3-4 Ja 158. (MINA 11:2)
1. Rachallnik shakhty N0.3 "Severo-Gundorovskaya" kombinata Sud&t-
antratait (Zhukov). 2. Predesdatell shakhtnogo komiteta shakhty
No.3 "Severo-Gundorovskava" kombinata Shakhtantratait (for Greahko).
(Coal mines and mining)

GRECHKO, D.I.
Improve the standardization prodecures in the Altay Territory.
Standartizatsiia 26 no.1:61-62 Ja 62. (MIRA 15:1)
(Altay Territory-Standardization)

'T
GRECHKOI D.I.; KOZHEVNIKOVA, G.I., inzh.-konstruktor
Standardization of accomqmnying documents. Standartizatsiia
29 no.6:4&49 Je 165. (MIRA 18:12)
1. Nachallnik otdela standartizatsii i normalizatsii Altayskogo
motornogo zavoda (for Grechko). 2. Otdel standartizatsii i
normalizateii Altayskogo motornogo zavoda (for Kozhevnikova).

8(0) SOV/112-59-4-7373
Translation froni: Referativ-ayy zhurnal. Elektrotekhnika, 1959, Nr 4, p 132 (USSR)
AUTHOR: Konokotin, G. S., and Grechko, F. M.
TITLE: Microthermometers
PERIODICAL: Nauchno-tekhn. byul. N.-i. in-ta mekhaniz. rybn. prom-sti VNIRO,
1957, Nr 3-4, pp 18-23
ABSTRACT: Electric thermometers with type MT-54 thermistors have been
developed for measuring the temperature of fish kept in stock, processed, or
transported. Injection needles of 0. 8 and 1. 5 mm diameter with built-in
thermistors are used for measuring the temperature inside the fish body. The
fish surface temperature is measured by a contact method. An unbalanced DC
bridge for two ranges (from -500 to -200C and from -200 to +200C) is used as
a measuring device.
M.A. K.
Card 1 / 1

, I ;
~-! F", ~, :`,P,
- _., I -
/) ,, /1, 1
SHLIKOVICH. B.M.; inshoner;
Somiconductive controlling and measuring Instruments. Nauka I pored.
op.v.sellkhos.7 no.1:26-28 Ja '57. (KM 10:2)
(Measuring Instruments)

GRECINO 1'. M.) Konokotin) S.G.
"Semiconductor-Thermo-Telemeasuring Devices. (20 pages, 1957)).Zavodskan
Laboratoriya, 1957, Vol,. 23, Nr. r), pp 1143-1.013 (USSR).

KOKOKOTIN, G.S.; GRBCHKO. Y.X.* MILLIR B.N., spetared.; LEVITSEATA, G.N..
red.; tekhn:red.
[Now semiconductor devices for temperature measurements in the
fishing industry] Novye poluproyodnikovys, termoizmaritellnys
pribory d1la rybnoi prorqshlonnosti. Koskva, Vses.nauchno-issle-
dovatellakii In-t morskogo rybnogo khoz. i okeanografii, 1959.
17 P. (KIRA 13:9)
(Thermometers) (Fisheries-Squipment and m*plies)

GRECHKO, G.S.[Hrechko, H.S.1p red.
[Possibilities for increasing corn yield; an accouirt of
the efficient workers of the collective and state firms in
Kharkov and SumW Province) Rezervy zbillshennia vrozhaiu
kukurudzy; rozpovidi peredovykiv kolhospiv i radhospiv
Kharkivslkoi ta Sums'koi oblastei. Kharkiv, Kharkivslke
knyzhkove vyd-vo, 1962. 50 P. (MIRA 17:11)

KLOCHKO, Petr Dinitriyevich; GRECHKO G H.S.1, red.;
~ J- -*i-,arechko,
LRANOVA, M. I. I norva tekhn. red.
ova.,
[Fattening cattle on a specialized farm] 'Vldhodivlia khu-
doby v spetsializovannomu hospodarstvi. Kharkiv, KharkivO-
ke knyzhkove vyd-vo, 1963. 24 p. (14IRA 17:1)

KAMYSHMI Aleksandr Pavlovich [Kor7shan, O.P ) g~g~' G.S.
Hrechko, H.S.), red.; LIMANOVA, M.I: fLymanoval-l"-T,71
takhn. red.
(Wide-spreadsovingof certified potatoes] Sutsillni sn-tovi
posivy kartopli. Kharkiv, Kharkivalke krorzhkove vyd-vo,,1963. 19 p.
(KIRA 17: 1)
1. Direktor sovkhoza "Berezivka",Kiiarkovskogo tresta
ovoslichno-molochnykh sovkhozav (for Karryshan).

MRTUSHM, Vladimir AniEsimovich; NOVIKOV, I~Iadijrir 'Vitrofmlovich;
KALUGIN, Leonid Konstantinovich; GHECHKO, G._S.[Hrechko,H.S.],
red.
[Prophylaxis of diseases in young "'am animals; aid to veter-
inary specialists and stockbreeders] Profilaktyka khvorob
uolodniaka sillslkohospodarslkykh tvaryn; na doporolm vete
rynamym spetnialistam i pratsiv-nykair tvarynnytstva. Kharlhv,
Kharkivs1ke kryzhkove vyd-vo, 1964. 74 p. (MIRA 18:2)

GRSCHKC , G. S. LF Hrtjchl-o, H. S. I I r,~id .
[Lp-rp,,p cropo every yearn t'!-.e of trie eff.'~ien--
wnrkers on collective anC oltate fa-rms in Kh!7.rkol; Provinl-11
fkl,v kolhos -. v
l,hjsokl vrozhal shchorokul rozpovid.1 perwir),~- yii
I radhospiv Kbarklvshchyriy. Kiiar'r,-.Iv, Kharkiv.,31ke knyz'hkove
vyd-vo, 1962. 82 p. 18. 1)

I-P -r , - ,-- - - ~ 2
., .., j"/ ~,- e,--,
i.~ X. 0
LUGOVOY, V.S.: LEVITOV, V.I.: VOLYNKIF, V.G.: GRECHKO, G.V.: APOST01ATOV, C.A.
T"Oft"UMMMEW
Experimental basis of electrotechnical.res,earch on the "Greater
Yqryn" project. Izv. AN Kir.SSR no.4:69-88 '57. (KW 10:7)
(Naryn river--Hydroelectric power stRtions)

-Plf~ LUGOVOY, V.S.; APOSTOLATOV, G.A.; VOLYNKIN, V.G.p- GROICHKO, G.V.;
vf ZIIUKOV, N.N. - ---
Factors to be considered in calculating and designing electric power
transmission lines in Kirghizistan. Izv. AN Kir. SSR. Ser. eat, i
tekh. nauk 1 no, 4:3-32 159. (MIM 1414)
(Kirghizistan-Electric lines)

G AT F Y
Al'S. JOUP. RZh'~j,,J., J,'c. 21 195,8, ~To.
AUT:,*~)R
-'T.
T
BST? ACT
CA ED
t
tit. J:-:r. -.-I. ir-l-A
v t i
io; t-9 o t' 0.%- i La :o zc;jo, j*-I I i, i
I V t..i!.V Ile,
a (11ij.
04 Pli
7t'l (lo.y.; is L~etot:-....fo uv e,~tc.--t
C Oil I N ]-A, P 7i!" -C L: -s
lect, iu ti'u
TO
).i sal, I, ).r)-Iy Lie .-,,s ,.ni
c.11 al;

S/181/62/004/001/025/052
B102/B104
AUTHORS: Grechko,-L. G., and Ovander, L. N.
TITLE: Peculiarities of Raman scattering in piezoelectric crystale
PERIODICAL: Fizika tverdogo tela, v. 4, no. 1, 1962, 157 - 162
TEXT: A paper by H. Poulbt (Ann. de Phys., 10, 908, 1955) is discussed
in detail. On the basis of the theory of pof-arizability, Poulet has
studied anomalies in Raman scattering and described the dependence of
Raman scattering on the wave vectors when longitudinal and transverse
oscillations occur in the crystal. In the present paper, it is shown
that the effects considered by Poulet may be due to intermolecular
interactions. The authors do not apply the theory of polarizability
whose applicability has not yet been verified for crystals, but consider
Raman scattering to be a polariton decay. They restrict themselves
to cubic crystals and triply degenerate oscillations. The contribution
of intermolecular interaction to Raman scattering is investigated, and
expressions are derived for the degr*ee of depolarization and for the
deDendence of the sdattering intensity on the scattering angle for
Card 1/4

S/181/62/004/001/025/052
Peculiarities of Raman scattering... B102/B104
in second-quantization representation and transformed to
r,,(~,-k 1) (2m I'x, 21) X

X (Ir jyjj 0) a(,)' (kJ ut~kj 0). (k. kj X
rM
B(2* (ki) (k2) B',!.) (k, k,),
X
(k):!:= IYjO e--"'".
r "aP [-L,
3.3 (6)
i'/I'kI, B' are Bose operators. HB can thus be expressed by production
a.na -!rinihilailon operators + using
7
E4, P~?
(k) P k) v (-k)],
BI (k) [E
(k) u;
,
v
P
3 M

GRECIIKO L ;-,VILEN!SKIY, Yu.B.
-! --.V -,
Contact fog in multilayer color films. Zhur. nauch. i prikl. fot.
i kin. 6 no. 3:225-226 My 161. (MIRA 14:5)
1. Filial Vsesoyuznogo nauchno-issledovatel'skogo kinofotoinstituta.,
Shostka.
(Color photography-Films)

BOGOLYUBSKIY, V.A.; SHCHUMELYAK., G.P.; GRWHKOP. L.V.; VILENSKIY, Yu.B.
Investigating the non-diffusing reducing agents for multilayer
color films. UBp. nauch. fot. 8:61-66 162. (MIRA 17:7)

7, -----------
3105816310001001
Ao62/Aiol
AUTHORS: Bogolyubovi V.,A., Shumelyak, G. P., Greohko, L. V., Vilenskiy,Yu.B*-1
- ------------------
.',TITLE: Ihvestigationof non-diffusing reducers for color multilayer films
PERIODICAL: Referativnyy zhurnal, Fizika, no. 3, 1963, 86, abstract 3D583
1962, no. 8, 61 - 66)
("Uspekhi nauchn. fotogr
0
TOM Non-diffusing reducers are employed in color films for removing ty
effects of theinteraction between emulsion layers; 1) the non-selective forma- J~
tion of dyes due to.the diffusion of.intermediate products of oxidation of the
developing substanoefrom~'Ithe layers, that contain dye forming elements with a
low reaction capacity, into the neighboring layers, and 2) the formation of a
higher fog on the contact boundary of emulsion layers with the filter layer of
colloid Ag (contact fog). There are described the results of the investigation
o" non-diffusing'reducers - derivatives of kydroquinone. It is shown that with
an increase of the number of carbon atoms in the alkyl substitution agents the A'.
.,diffusion stability and the antifog,aotion Jiiorease from 2,5-dibuty,1hydroquinone.
,-_:-,':.to 2,5-dioctylhydroquinone, and.then somewhat.decrease because of the bad solu-
Card 1/2

S/058/63/boo/bo3/04/lo4
Investigation of.:non ffusing reducers for- Ao62/Aioi
;.-bility of the dialkylhydroquinones. The same lasr.was observed In a number of
.,.2,5-bis-(dialkylaminometh-yl)-hydroquinones; however the application of some
I'dialkylhydroquindnes and 2,5-~bis-(diaikylamiiiometliyl)-hydroquinones was limited
.-::.by.the formation of dyed-compounds in their photographic processing. There was
the formation.of dyed compounds from 2,5-diallqlhy&,oquinones and 2,5-
--:,-,-bis-(dialkylaminomethyl)-hydroquinones and the purple component 1-(4-pheno)W-
~'~:,-3-sulpho~henyl)-3-octadecylpyrazol6ne-5- It is established that the formation
,.~,_reaction of the dyed compound takes place at -the Ag bleaching stage of the image J
l'by potassium ferricyanide. When t
reating a film, that contains a non-diffusing
!_~reducing agent; x1dation of.the film to the corres-
by potassium ferricyanide, o.
i~ponding quinone-takes place.--, There are described the chemical structure and
.~~_~~spectral properties of some'dyes which are formed at the interaction of-that
7 ~._,quinone with the-dye forming components.
D. Balabukha
[Abstracter's note: Complete translation]
-,Card 2/2

RAMMOVSKIY. V.G.; GRECHKO, M.F.
Investigatinj1particular methods in evaluating the smoothness
of surfaces. Trudy VNIIN no.12:122-132 151. (MIRA 11:6)
1(Surfaces(Tachnology)--Standards)

GRWHJDDV XJF._ . ~
/-~ ~,Zvsff-tlg-ailon of the PIU-1-type interferometer. Trudy MIN no.18t
48-55 152. (mm li-W
(Interferometer)

GRECHKO M.F.; SNIRNOVAP L.I.; STRAKUM, G.I.; SHAROVA, Ye.Ye.
-
Standard device for measuring angles. Trudy inst.Kom.standpoper i
izm.prib no.47:127-138 161. (MIRA 15:12)
1. Voesoyuznyy nanchno-iasledovat4l'skiy institut metrologii.
im. D.I.Mendeleyeva. jooniometere)

al KIY, I.K-; VILENSKIY, Yu.B.; GRSCHKO. U.K.
Relation between the total resolving power and the resolving power
of the individual layers in multilayer color film. Zhur.nauch.i
prikl.fot.i kin. 1 no;5:359-361 S-0 156. (K6u 9:11)
1. Vessoyuznyy nauchno-inaledovatellskiy kino-fotoinstitut i
fabrika kinoplenki no.3-359-361 S-0 '56. (MLHA 9.11)
(Color photography)

. . . . . . . . . .
621.5-~5- E4T ii) /gi(P(j Y SSD/AEDG(a)/A-SD(a')-5/&W ESD(
ACCESSION NR: AR4039918 S/0058/64/000/004/DlIS/DI16

S 63

,
d t:,-1 O'f potassium thiocyanate on:
The effe 066/A126
A
q
amounts of ammonia (0.044 mole/1).onl-the tendency~b aggregation on the
surface of silver halide.- Thd two.4117stateso- which increase the red sensitivity
d
of the adsorption la~rer bonsiderably, are attribute to the presence of thiocy-

s;' anate in-the emulsion. There are 2.figures'and I table.
j
ASSOCI TION: Filial NIKFI Shostka (Branch of NIKFI,.
A ShostkiL)

SUBMITTEM June 11 1962'

Table i Properties of~four emulsions. 1 NumbRr of emulsion; 2 CNH mole/I)
2
ion'..~~*4; 5
mean crystal size, Itc, 4 - dispers
'
CA4, mole%; 6 CA90
after second ripening!
&/I of emulsion;. 7 emulsion

C

PeARUR - PAS-

aCT&JI.
x

ep-
jlncn

A91. pnr
PH

.
map
P

wt
% t1A
mq
A40A61A - -CR
SMIM apapa
yoro co

.1
0 70
'1337 0,58 31
40
2.5

11
0, W
t:88t
2-39
,0,7
(IT 7,2 3,5

'.III
~O 44 0.505
13
0. 3 -24
5,0 7.0
3.3

V

0 0 3A 6 0 5; 7

Ei
M 7.2
3,3
Card 2/2