SCIENTIFIC ABSTRACT NAMETKIN, N.S. - NAMIRSKI, P.N.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001136020017-0
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: January 3, 2017
• Document Release Date: July 31, 2000
• Sequence Number: 17
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

'W! P -4 /Pr -4/ a -4 PJ~
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A'7'z- Name 1- N~nrras nond inz member AJI Vd ovin, W. M.
p0 va,
to
SOURCE: Ali SSSR. Doklady*, v. 159, no. 1, 1964, 146-149
9 eM. ~q
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a, tiv 1, t v, D r jzs n' s yT., ~,:~a s i s~zy ~i,-9e
--!s -w:r~ 4s a --art a s--u-4v on the 'ri-luenc-i of lifferer* ra"Icals
~n
r9a
size) and its comparison with the activity of the respective opfin chain analogs
were a1sc of interest. It was found that the addition reacLion of hydr-ide jeriv-
a',179 .' - --n-- -P~r 'oo-~ -3*
, /3
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ACCESSION UR: kF4049139
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Orig. art. has: 3 tables and 3 figues-
A3-3~:;C -A- sinte7a Akademil nauk SSSR (Institute
Aca-Jew
C.CDF X NC ~i-FF SCV 004
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Fig.
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TOPCIIIYEV, ILIeksandr akarlem!'el(deceased); KARGIN,
V~A., akndemik, o-'Iv. red.,; SHTMI, V.7a.,. dok+or khim.
natkil ct-v. red.; SPCENOV, N.N., akademik.. rad.;
ZHAVORONKOV" II?.M.p akaderaik;, red.; NAPISTIKIII, N.S., red.;
SHMIN, N,I,v red.- LIKHTENSIHTONT~Y
nauk, red.~ KU7113.r-QbV,: V.I., red.
[Selected works] Izbrannye trudy. Mos"rap Nauka.[Bcok 11
1965. 427 p. (MIA 18.8)
J. Chlen-korrespmdent; &N SSSR for Nametkin., Shtrjkin).

Card 1/2

Cord 2 /2

L 61648 -65 E~7 (m) /EFF (c /3, pj/T PC-4/,Tlr-.u M4
,m IR. am -1,;, V. I.; Grinberg, P. L.
V(Iovin, V. M.: ZavI Va lo,.
SOURCE: AN SSSR. izvestiya. Seriya Khimtclieskaval ao.
ganor,filcor, co=ound, sili ocvc!obu!sne
TOKC ":.AGS;
--,-.-rArivp nt the dlisillcoc-lclo-

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7 1 1
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Card
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Card 2/2

LUTES, L.A.$ PINKELISIRT-PYN, Y,-.,.Sh.; VPOVIN, V~M.,_LAYIMI , N.s.
,L
Ramman spectra of some ortho-substituted benzene. deriva~ 'i-ves contafnirg
silicon. Izv. All SSSR. Ser. khim. no."W305-11-08 '65- (PURA 1817)
1-Institut organicheskoy kh-imii im. N.D.Zelinskogo P.N SSSR,

90 C, ~ c ~TWAM
L 5 2 1-0 1 Ef A,
ALrrHOR: Nanietkin N. S 7dov M.
Iy, ;,Mj r
T 7T.E: r ri )es. C !ass
2f,

1700-&
L EWT (m) /EPI? (c) /EWP (j /T
ACCESSION NR:' AP5022932 tm/oo62/65/ooo/008/1448/1453
546.28T.542.952
-AUTHOR: Nametkin, N. S.; Vdovin, V.M.; Zav'yalov, V. I.
TITLE: Po riiati 1,1-disubstituted silacyclobutanes
ISOURCE: AN SSSR.-,Izvestiya. Serlya khimicheskaya, no. 8, 1965, 1448-1453
TOPIC TAGS: tilane, polymerization
ABSTRACT: In an attempt to prepare heterochain silicohydrocarbon- polymers, a
study has been made of the polymerization of 1,1-disulistituted silacyclobutanes
.(see formula below), The polymerization1was carried out without catalysts at
.150-200C at stmospheric.pressure or in sealed ampuls. On the basis of IR data,
the,.reaction was assumedto proceed thus,:
R' C111
C114 Off MIN Ofs Of, Clio CHI ECAM
Me C.Ifs a-Ciffe 01-CH, MCH-0f. QW,49. CA %ff,

L 1700-66
ACCESSION NR: AP5022 .932
A regular structure was assigned to the polymers on the basis of the crystalline
structure revealed by x-ray analysis, IR spectroscopic data, and substantial
mal-oxidative stability., The-polymers were solid, slightly elastic or rubber-like
materials, semitransparent or white in color,and, as a rule, soluble in the commonl.'
organic solvents, Viscosity, molecular weight, melting point., and glass transitionf
temperature data as well as x-ray patterns and DTA curves are given for some,.of the,
polymers. Orig. art. has: 3 formulas, 5 figures, and 1 table. [SM]
ASSOCIATION: Institut neftekbimicheskogo sinteza im. A4 V. Topchlyeva Akademii
nauk SSSR-(Institute of-Petrochemical Synthesist Acadeaw of Ocienges)B88R)
SUBMITTED: 28jun63 ENCL:. .,00 SUB CODE: .--"j
No REP SOV: 009 OTHER: 001- ATD PHESS:q0?3
CQ

L 1448-66 &T m)/EPF(c)/3-1P(J)/7' RM
1ACCESSi NR: ~AP5022933 uR/oo62/65/000/oO8,(l453/l459
546~g87+542.952
AUTHOR. Nametkin .-S.; ovinl-V. M. Tiishch6vaya K S. ;. Zav yalov, V. I
~'Zolymeriiation%f 1,1-disubBtitute*&'-silacyclobentanes
TITLE
SOURCC.: AN 668R. Izvestiya, Serlya-khImichesk a, no. 8, 1965) 1453-1459
(1y
TOPIC TAGS: silanej Rolymerization
ABSTRACT: A study has been made of the catalytic pofymerization of 1,1-disubstituteid
silacyclopentanes of the type
n, - MIS
SKCIT
Where n 2, and R and R' are alkyl, aryl, substituted. alkyl, chloro; or hydrogen
radicals. The reaction-was carried out at atmospheric pressure and 2C~_120C with
1 AlC13 catalyst. Itwas found that silacyclopentanes vith alkyl or hydrogen sub-
stituents polymerized to form heterochain silicohydrocarbon polymers. The pol~mers~,
Were colorless, highly viscousg soluble in the common organic solvents, and had mo-
lecular weights of I x 103 to 2.5-x 103 Bis( hylenesilyl)ethane formed
methylte-tramet
ard

-'ACCMSION NR: AP5022933-
an insoluble tri(limensional netvork product. Based on spectroscopic data the reac-1
tions. were'assumed to proceed as followst.
11-:01clilCHICH
R, 0113 - CHI
M
R-Mls, R'-Cffs: R-Cff..,
R=11, R'-Cffs
CHr-CHS CM C1111_. CH. H~C IMIS
A
HICHS
\(CHI),
On the other hand, silacyclopentanes.witk chlorine.' phenyl, benzyl, or substituted
trizability was inter-
alkyl radicals did not polyineri.ze. Tliis difference*in polyme
pretea in'terms of differences'in the interaction of the cyclopentanes with AlCl
3
Of all the polymers prepared,:tb.at,of 1-bydro-l-methyloilacyclopentane was of spe-
_!Pard 2Zj

t;'~ T W /9PF (c Vr/
LM, 99-66
ACCESSION NR: AP5025505 UR/0062/05/000/009/1547/1553
543.4:22+546.287
AUTHOR: Nametkh!,.N..,,,g,; Oppengeym, V. D. ZavIyalov, V.-L; 1~uskch2,.~a v~, 1. S.;,
Vdovin, V
4
TITLE: Infrared absorption spectra of 1, 1-substituted aillcocyclobutanes, ilico-
cyclopentanes j and corresponding polymers
SOURCE: ANSSSR. Izvestiya. Seriyakhimicheskaya, no. 9, 1965, 1547-1553
TOPIC TAGS: organosilicon compound, polymer structure, IR spectrum
ABSTRACT: The study alins at determining the frequencies of the absorption band maxima
Pliaractcrizlng a 4- and 5-niembered beterocyclic ring containing a silicon atom.' T110
characteristic frequencies obtained were used to elucidate the structure of polymeric
products obtalned by thermal polymerization of -1, I-substituted silicocyclobutanes
CI! /R1
C11 and 1, 1-substituted sillcocyclopentanes St.
~Rl
J ~,C[12 112 C11j R1 I
CAN -jl3L--
n 0 2 cl

L 5095-66
AccESSION NR- AP5025-505
IR spectra of the polymers obtained from the silicocyclobutanes showed that the' polymeri-
.zation products are heterochain polymers with the structural fragment
Rt
(CII (CH as the link of the principal chain. Products ~obtaincd izcm 1, 1-
2)3S1 2)
substituted silleocyclopentanes are heterochain polymers with the
structural fragment ~Ml W
a;s the link of the
81 (CH2)48L (CH2)4-
principal chain.
Orig. art. haB: 5 tables and 5 formulas,
Card: 2/3

L 5095-66;,
ACCESSION NR: AP502550.5
ASSOCIATION: Institut iir,-ftelddmlclxcskogo sinteza im. A. V. Topcliiypva Ahademil naulc
SSSR (in3titute of Petrochemical Synthesis, Academy o~ScicEn.~SR)
SUBMITTED: Wtuif33 ENCL: 00 ~UB CODE: 0 C, 6- C
-NO RE F SO V: 008 OTHER: 003

L 3685-66
EWT(m)/EPF(c)/~WP(J)/r/EVIA(C) RM
------ -- -0/600/65/166/006/1- 0-87/1089
ACCESSIONIM: A0~661!
% no
AUTHOR.'- Nametki N. S.f.C6rresponding member AN SSSR),Perchenkog V. no-, Batalova',
L. Go
TIELE: Cyclodimerization.of N-ethyleniminos lane
SOURCE. AN SSSR. ~Doklady* v. 160, no. 5, 19650 1087-1069
ompound, organic synthetic process, silane polymeri-'-.:.
~TOPIC TAGS.- organic Imine C
Vition
ABSTRACT: Thermal transformations of N-ethyleniminosilanes,
CHI
3
C112
studied. The experiments were done at 200, 250 and 3000 in sealed ampules. At
a
re
:2500, triethyl.ethyleniminosilane undergoes transformations which result in the z'
formation.of N,K-I-bis-(triethylsilyl)-piperazince Dimethylphenyl, methyldiphenyl.-
mothyldibenzyl j -diethylphenyl and'ethyldietho- ethyl ans
XY eniminosilanes undergo tr
formations in similar cofiditions with variounjields of N,Nl-diallyl-substituted
ie
piperazines, ..The naturevf.silicon radicals has a considerable effect on the
y
'Card 1/2

7 7,
-3085--oM
ACCBSSION NR:. APS007565
of cyclodimerization products. Triethyl ethyleniminosilane at 3000 forms N,N1_
bis-(triethylsilyl)-pi zind Nl-bis-(triethyltilyl)-ethylamine--and'deeper
pera N
onversion products
C -0110,
(0114), 81-N 14-~Sl (CIU.").
V
+ (CjHi)j Sl~-N_81 (CqHj)*
If
The presence of condensation products and N,N'-bis-(triethylgilyl)-ethylami e'in-
n
dicates that saturation takes'place'due to dis ' ortionation-of hydrogen.. A
Prop
table is given showingit of N Ml-bis-(dllyl)-piperazines. These com-
he properties
pounds are separated fro6~the reaction mixiure'by fractionation in vacuum. Origi
art. has: I table., h1mUhaskog6 _Inteza b opc
4-- T
ASSOCIATION:', Institui neftek A hiyeva Akademii
-nauk SSSR (Institute of Petrocheinical SVthesis, kadeati j~f. Scien!zgg4
Lt - 00
ERC ~Su
-SUBMITTED*.--- 1SSep~~'. B CODE: OC, GC
-NO Fxr sm: ool
card-

5u,'-6 AF N C 'S.
C. r

11AMETKIN, N.S.; VDOVIN, V.M.; ZAVIYALOV, V.I.
Silylethylene elastomers. Vy6okom. soed. 7 no.4:757 Ap 165.
(MIRA 18: 6)

T-P ri i CA ir r~
TOPIC TAGS vinvlsiloxane rr))vmer!7:o!-~

U
mA
L L2L-6-5
ACCES:31ON NR: AP5020969
polvme-izatinn vipld w-i~ rc-riiwnri 4c
V 1~1 the m,)n-ti;er. Orle A i -t h. ;L q A i Lri rp
NH

- - ~ - ... I ' t
tl- .'
f! . r : ; . - ~ 1 C -, a PL 17C _,. ra._' '-:-a; -~c -pier,- zz L;-,, r - 1'. - - '~- ylqi~. . ~ & -

1-1
Ai;k;z661vh lia. A~l ~FV'Lu'l. kAj I
I

I a

BIRYUKOV, I.P.1 VORONKOV, M.G.; BABIGH, E.D.; ARKIIIFOVA, T.N.; VDOVIN, V.M.;
NAMETKINI N.S.
Nuclear quadrupole resonance of 1,1-dichloro and 1-methyl-l-
chloro-l-silacycloalkanes. Dokl. AN S,"),31t 161 no.6tl336-1338
Ap 165. (MIRA 1815)
1. Institut organicheskogo sinteza AN LatvSSR i Institut
neftekhimicheskogo sinteza im. A.V.Topchiyev'a AN SSSR.
2. Chlen-korrespondent AN SSSR (for Nwnetkih).

A R~'Ill~tkf- * 7 .1, '. . ' 00n(l ill ' -k f-el .11Y -f-IT11.17-Iflu j -~, I "A-

armia.m.-M, R

.Peli-~,~)9*1-~InI.P.,L-~LIaL,4fl7w-VKLlg~-~ mill?m

~r !IT

METKINY N.S.; PRITUILA, N.A.; CHERNYSIONA, T.I.; ZI!AlMENM&A--,- E.-N. ---- - - - --- -
Synthesis of 1,4-bis-(dioi-ganovinylsilyl)-benzenes. Dokl. A21 SEZR
164 no.6:1319-1322 0 165. OaPA 18: 1c),
1. Institut reftekhimicheskogo sinteza im. A.V.Topchiyeva AN SSSR.
2. Chlen-korrespondent AN SSSR (for Nametkin).

L 3188h-66 EWT(m)/EWP(J)/T RMIWW
ACC NR; AP6012538 SOURCE CODE: UR/0062/66/000/003/0584/0585
'AUTHOR: Nametkin, N. S.; Vdovin. V. M.; Gusellnikoy.,, L. ~e.; qav!X21�~ . I.
JL_
ORG: Institute of Petrochemical S~nthesi�
SSSR (Institut neftekhimicheskogo sinteza, Akademii nauk SSSR)
TITLE: Formation of 1,3-disilagyclobutanes in protolytic condensation reaction of
1-silacyclobutanes
SOURCE: MI.SSSR. Izvestiya. Seriya khimicheskaya, no. 3, 1966, 584-585
TOPIC TAGS: organic synthesis, silicon compound, condensation reaction
ABSTRACT: 1,1-dimethyl-l-silacyclobutane was passed in a stream of heliuithrough a
quartz tube, 14 mm in diameter and 200 mm in length, heated to 6000C at the rate of
3 g/br. The rpetion mixture consisted of gaseous and liquid products. Gas-liquid
cbromatography(and IR spectroscopy showed the gaseous products to consist of - 95%
ethylene and - 5% methane. As a result of separation by distillation, it was es-
tablished that the condensate contains unreacted monosilacyclobutane and 1,1,3,3-
tetramethyl-1,3-disilacyclobutane, produced with -55% yield. The disilacyclobutane
Card 112 UDC: 546.287 t 542.954

L 31884-66
ACC NR: AP6012538
obtained has the following characteristics: b.p. 118-1200C, nD20 1,41111; d,10
0.7988, m. wt. 139. 1,1-dichloro-l-silacyclobutane was similarly converted to
'crystalline 1,1,3,3-tetrachloro-1,3-disilacyclobutane at 6800C with high yield. The
gaseous product consisted of only ethylene.t
SUB CODE: 07/ SUBM DATE: 28Dec65/ ORIG REr: 001/ OTH Rcr: ooo
'Card 2/2--J~0----

L 37211-66 _E'NT(m)/EV1P(j) ' RM/JW
ACC N" AP6014410 .SOURCE CODE: UR/0062/66/000/004/0737/07381
AUTHOR:,Nametkin, N. S,; Grushevenko, I. A.; Ferchenko, V. No
ORG: Institute of Petrochemical Svnthesis im. A. V. TopchiYev Academy
of Sciences SSSR (Institut neftekhimicheskoao sinteza, Akademil nau
TITLE: Reaction of ethylenimineiwith allylsilanes
SOURCE: AN SSSR. Izvestiya. Seriya khimicheskaya,, no. 4, 1966, 737-
TOPIC TAGS: silane, organic nitrogen compound, chemical reaction
ABSTRACT: The formation of an addition product of triethylallylsilane
and ethylenimine was achieved in 35% yield using ethylenimine amide as
catalyst. Addition was at the beta-carbon of the allylsilane. The
presence of the phenyl radical at the Si atom of the silane leads to
breakdown of the Si-C bond. Thus dimethylphenylallylsilanelformed no
addition product with ethylenimine, but gave dimethylphenyl-N-
ethyleniminosilane and propylene. Orig. art. has: 2 equations.
SUB CODE: 07/ SUBM DATE: 07Aug65/ ORIG REF: 002
hyZ141 UDC: 542.91k547.233046.287

Vrr(-*-)/PV1D(j1/T- . YTDIPI
1, 2~Z52-66
TACC NRs AP6010111'. SOURCE'CODEj/0190/66/008/003/0476/0480
AUTHORSs Sorokin, G, V.; Nametkin, No S*; Perchenkop Ve Ns__
ORG:. Institute of-Petrochemical Synthesis, AN SSSR (Inatitut nefte-
khimicKeskogo..sinteza AN
TITLE.:. -.P61 6erizatio oi-ethyleneluaLng TiC14 + Al (isO-C4H9 .)3 cat:sly
in* the presence
o. 3, 1966, 476-480
SOURCE,. Vyookomolekulyarnyye aoyedLneniya, v. 8, n
TOPIC TAGSt ethylene,, polymerization catalyst, polymerization rate,
silane, chain polymerp polyethylene., silicon
ABSTRAM The effect of silanes of various structures on ethylene
polymerization with TiC14+ Al (i80 C4H6)3 as a catalyst was analyzed.
The maximum polymerization rate was observed at the equimolar ratio of-*~:-
the Al(isO-C,4H9)3 and allane. The activation effect.of silane with
one hydrogen at the Si atom Is much higher than that of silanes with
two hydrogens at the Si atom, which could be explained by the'chain
termination caused by.the entrance of corresponding silanes with two
'hydrogens into the polymer chain. It was shown that the.content;of Si
in polytethylene samples prepaved with TiC14+ Al (isO-C4H9)3 depends
on the nature of.silanes,, Orig, art. hass 3 figures and 1 table.
rd 1/2 66,095.26+678*742
C-0
L

A -CC-N-R, AP6610Ia- (A) SOURCE CT9: UR/0190/bb/0081003/05531055b
.11 AUTHOR-- -Konobeyevskiy, K. 'S. Cusel Inikay, L. Nametkin, N. 8.6 Polak. L. S.;
Chernysheva, T.
Olk0i _.Jnatitute of Petrochemical gynthesis, AN SSSH (Institut neftek-hfi~diheokogo?)
;.,binteit-AH SSSIR)...
TITLE1 ':.Anvest igition of radiation X21mrizationlf Vinyl-illoxanes
.SOURCE: :Vysokomo1ekulyarnyye spyedineniya, Y'. 8, no 3i 1566.o 553-556
TOPIC-TAGS: radiation polymerizationj vinyl siloxanet..* Aloranep monomert-polymer,
-,.styrene-#, graft copolyMer
Gamma:
ABSTRACT: The paper deale vith.ia:diolysiso*polym-,erization,*and the effect of
:rays on monomeric-Tiol vinyl ..s ,ilo*xanes. The existen6e of stabilized, free,.','
_ yfunctional
radicq.1s confirms its microgell.%ature. ~ 'The possiltility of pre - ing grift copblyweri,'
par
..is demonstrated by-initiatingfityrene polymerization with microgel ofA .3 5-tri-_
vinyl-lo 3,'5-pentamethyltrl'iiloxa"'n~~ Orig. art.:.hast".3 'figures and I t~iblijli`~ (Based
'on-authors' abstract.).~ WT),
-SUB.-qODHf".- -07[ 0("..DATZfo-~ ~4ftr65/ 01iIG'MW. ,002/..-, OM REF:. - 006t;
A.
:UDC
(3 L a, mosts 745
Co

~-L-3266,3-66-- ---EwT(m)jkwP-(j)/T IJP-(C-) - WW/RM-
ACC NRiAP6015053 uRluIvu!66-/-008"ur5-tag8g-/(Y892
(A) sOuR" P"T.-
AUTHOR: Nametkin, No..S.; Nechitaylo, N. A.; Durgarlyang So G.
Khotimskiy 0... ve so F3
i ORGt Institute of Petrochemical Synthesis, AN SSSR (Institut nefte-
khimicheskogo sinteza AN SSSR)
TITLEs Thermal stability of polymer from vinyl derivatives of silicon
:i SOURCE: Vysokouolekulyarnyye moyedinentyag v. 6, no. 5, 1966, 888-692
TOPIC TAGS: polymer, silicon, silane, macromolecule, thermal oxidatio
oxidative 'degradation., TWroe--"#q..e- b0aoeAD*1-r,10AJJ 7-,V46iemqA.
ABSTRACT: A number of macromolecular orlanosilicon polyneralhaa been
synthesized from silicon vinyl derive ea. The stability of synthe-
sized.polyvinyl silanes was analyzed by the differential thermal metho
Th t bilizer effect on the process of the therpooz14stive degrade-
n a
-Meon3of the-polyvinyl trimethyloilans was shown, Orige art# has: 4
figures and I table. INT)
SUB CODEI 11, 07/ SUBN DATE: 20May65j ORIG REY: 004/ OTH REIF:- 001
Ler UDG: 678.01:54+678.84
Card 1/1

L 32659-66 EWT(m)/EWP(J)~T 1JP(c) RM
ACC NR:AF6015057 (A) SOURCE CODES UIVO190/66/008/005/0921/0925
AUTHORt Nametkin, N. S.; Ghernyshevaq T. I.j. Pritula, N. A.; Znamenskaya, S. N,
ORdi Institute of Petrochemical Synthesis, AN SSSR (Institut neftekhimicheakogo
sinteza AN SSSR)
TITM Oligomeric organosilicon compounda with 1~henylene"Ilnko
SOURCE: VyaokomolekulyarWe soyedinaniya, v. 8. no. 5, 1966" 921-925
TOPIC TAGSt acoty;Lene, benzene, j=1Xmwnj polymer chemis.tryq organosilicon
compound Alw.F,9,,P- Av&Pmre 04490"7eoc
9
ABSTRACTt Faemplifiqd by the interaction of 1.4-bis-(diorganosilyl) benzenes with
acetylene and 1.1+-bis-(diorganovinylailyl) benzenes wilh silicon dihydroderivatives,
the principal method of obtaining the linear polymerlc~3products with phenylenecarbon
and phanylen silicon1lines was demonstrated. Orig. art. hast 3 figures and 1 table.
INT)
SUB CODEs 11.. 07/ SUBH DATFi 24May65/ OBIG JW2 Oll/ OTH RHF1 005
Card I /I

ACC NRi AP6010122, SOURCE CODE: UR/0190/66/008/003/0557/0559
AUTHOR: Bokeno Yu.; Gusellnikov, L. Ye.; Nametkinp N. B.; Polak, L. S.; Chernysheva,
T. I.
ORG: Institute of Petrochemical Synthesis, Academy of Sciences SSSR (Institut
neftekhimicheskogo sinteza AN SSSR)
f
TITLE: -Radiation-induced polyme zation'of polyfunctional al~ ~ilanes
SOURCE.,, -Vysokomolekulyarnyye soyedinediya, v. 8, no. 3, 1966, 557-559
TOPIC TAGS: radiation polymerization, radiation effect, temperature effect, con-
version rate, monomer, silane, allylsilane
ABSTRACT: An experimental study of the effect of solvents, dose rate, and temperature
on radiation-induced polymerization of diethyldiallylsilanes (DEDAS) was made. The
dependence of shrinkage of the system on the radiation dose, in the process of
radiation-induced polymerization of various diallylsilanes, was determined by the
dilatometric rate of 2.5 ml and the scale value of 0.01 ml at 25C, and the dose rate
of 350 rad/sec. The shrinkage of the DEDAS system at the dose rate of 700 r/see
and at 50C was determined by the dilatometer scale rate of 0.005 MI. The effect of
solvents was determined by comparing the yield of a polymer in the presence of
solvents to the yield of a polymer in bulk polymerization, using the same dose of
radiation. The dose rate and activation energy were plotted against the monomer con-
Card 1/2 um 66.095.26+678-745

e
ACC MR: AP6008083 (A) SOURCE CODE: UR/0020/66/166/005/1118/1120
AUTHOR: Nametkiti.,.N.~,S..(Corresponding member AN SSSR); Khotimskiy, V. S.;
Durgarlyan,78-.- G. 50
ORG: ~Institute of Petrochemical Synthesis, AcadeTy of Sciences SSSR (Institut nef-
tekhimicheskogo sinteza Akademii nauk SSSR)
TITLE: Synthesis of high molecular Rolyvinyltrimethylailane and some of its pro-
perties
SOURCE: tAM SSSR. Deklady, v. 166, no. 5, 1966, 1118-1120
TOPIC TAGS: silane, organosilicon compound, polymer, organolithium canpound ,
organic synthetic process, high polymer$ hydrocarbon
ABSTRACT:: The paper reports onthe synthes a of-a high molecular polymer from
vinyltrimethylailane-In~cyclohexane In the presence of.butyllithium. Ultimate ana-1
lysis and infrared spectroscopic data lead to the following structural fomula of
the polyvinyltrimethylailane obtained:
ffl-~ 1--CH8
Card 1/2: UDC: 041.64

L 1891"
ACC MR: AP6008083
A study ~ of the thermomechanical behavior of this polymer over a wide temperature
range bowed that it is a vitrified substance with a glasd-transition temperature
above 2000C. ~, It -has a relatively high -thermal stability. Introduction of 3 to 5%
of the antioxidant phenyl-B-naphthylamine substantially raises the temperature of
the start of themooxidative degradation (from 245 to 3400C), and decreases the
rate of oxidative processes as- indicated by exothermic peaks on the corresponding,
beating curves. The polyvinyltrimethylsilane synthesized is a representative of
a new.class of high molecular silicon hydrocarbon polymers obtained by polymeriza-
tion,-at the.unsaturated bond of-the vinyl group at the silicon atom. Orig. art.
hasv~ 3 figures, 1 table.
SUB CODE: 07/ SUBM DATE: 3OJul65/ ORIG REF: 004/ OTH REF: 004
Card 2/2 M

RM
-66
U
NR, AP6009489 R/0020/66/10/001/0106/0108
"AUTHOR: Nametkin, NaS.(Dorresponding member AN SSSR); Perchenko, V.NL;
Grueheve11W-.-Z'-A-,KMeva, G.L.
ORG: '.Institute of-Petrochemical Synthesis Im. A.V. Topchiev AN SS$JL
(Instrtut__ig?tekh1m1chesXogo sluteza AN SSSRY
TITLE,: Addition of amineowith various struoturea to vinyl allanos
SOURCE: AN SSSR. Doklady,v.167, no.1, 1966, 106-108
TOPIC TAGS: ellane,I amines chemical reaction, heterocyclic baBe compound,
primary.aromatic amine, primary aliphatic amine
ABSTRACT: The aim of the work was to investigate the possibility of the
addition to triethyl vinyl vilane of other heterocyclics, as well as
aliphatic and aromatic amines-'-diethylamine, u-propylamine, piperidine,
pyrrolidine, monomethylanilin, and: pyrrole. The article gives a detailk,
description of the laboratory,procedures used to synthesige the follow-
ing compounds: ja -(N-n-prop agine)-ethyltrleth6 silane 18 -(N-diethy..
lamine)-ethyltriethyl sliane; fJ -(N-piperidyl)- y1tr1e 71 silane;
and, )3 -(N-piperidyl)-ethyltriethyl silane. Synthesis with monomethyl-
anilin and pyrrole were carried out under analogous conditions in the
presence of metallic lithium and of previously prepared amides of pyrr-
L,q.3rd
uDc-. 547.1'3

NAMETKINAP A. M.:
NAMETKINAY A. M.: "The affect of phenamine on the higher nervous activity
of dogs of various types of nervous system". Moscowj 1955. Inst of
Higher Nervous Activity) Acad Sci USSR.
(Dissertation for the Degree of Candidate of Medical Sciences)
SO: Knizhnaya Letopist No. 51, 10 December 1955

NAMUKINA,
Affect 0 Phenomine on the higher nervous activity in dogs with
different types of nervous system. Report uo.le Trudy Iust.yys.
nervedsiato Ber,fiziol. 1:96-113 155. (MIRA 9;8)
1. 1z laboratorii vagetativnykh uslovnykh reflsksoy, zaveduyushchiy
K.A.Usiyevich
(PIMNETRYLAXIEN) (PSYCHOLOGY, PHYSIOLOGICAL)

NAMRTKINA. A.M.
31 phenomine on the higher nervoue activity in dogs with dif-
feront typos of nervous systems. Trudy Inst,vys,nerv.delat. Ser.
fiziol. 2:146-156 056. (KLRA 10:1)
1. Iz laboratorii vegetativrqkh uslovnvkh refleksov, Ispolnyayushaya
obyazannosti zav. - A.A.Pavlovskaya.
(PUMMINE) (TIMPMMENT) (CONDITIONO RESPONSH)

RACHVELISHVILIP B.Kh.; WIGAUDZE, N.E.; GOGNIASHVILI, Sh.l.
Endobronchial treatment of the nonspecific abscess of lun. s Soob. AN
Graz. SSR 32 no.2-477-482 163. f;iF~ 181l)
1. Thilisakiy gosudarstvennyy maditsiniskiy institut. Sii=itted March
15l 1963.

NAMGALADZE, P.B.
' ZU;a7;n;;g7:s;U;1;11g wells as regulating reservoirs in rain-water
canalization. Trud7 GPI no.6:93-96 '56. (MIRA 11:2)
l.Kafedra vodosnabzheni7a i kanalizatsii Gruzinskogo politekhni-
cheskogo institita im. S.M. Kirova, Tbilisi.
(H7draulic engineering)

ITANGLADZE, T. D.
"Data on the Problam of Laboratory Methods for the Investigation of Certain
Thread Funei.11 Cand Med Sci, Thilisi State 11-ledical Inst, Tbilisi, 1953. (RZhBiol
110 5, Nov 54)
Survey of Scientific m-d Technical Dissertations Defended at USSR Higher
Educational Institutions (11)
SO: Sum. 110. 521, 2 Jun 55

GORBUNOVA, N.A.; NAMIATYSHEIVA, A.M.
0
Ukeet of antithrombocytic serum on the functional state of the
coagulation system in dogs. Frobl. gemat. i perel. krovi 5
no. 12t28-36 160. (MIM 14:1)
(BIDOD-COAGULATION) (SERUM)

NAMICHEV, 4,'%dots.; STEFANOV, St.
Clinical analysis of 30 cases of brain abscess. Khirurgiia
(Sofiia) 16 no.7:607-611 163-
1. Vissh meditsinski institut "I.P. Pavlov" - P:Lcrvdiv, katedra
po nervni bolesti i nevrokhirurgiia~ Rukovoditel na katedrata:
prof. Tr. Zaprianov.
(BRAIN ABSCESS) (CEREBELLAR DISEASES)
(BLOOD CELL COUNT) (EPILEPSY)
(CEREBROSPIDIAL FLUID)

KITOV,D.; NAMITCHEYY.[Namichev., I.]
Giant spiral meningiom of the spinal cord. Folia med. Plov-
div) 6 no.2tl28-132 164
1. Institut de Hautes Etudes Medicales *I.P.Pavlov* do Plovdiv,
Balgarie; Chairs des Maladies Nervouses st do Neurochirurgie.
(Direateurt prof. Tr. Zapryanov [Tr. Zaprianorl).

-mv-- L-r, 0. 1.
NAUICHEMMU, G. I. - "Acquaintance ~Jith agricultural techni-,uez; in
the process of -Audying j*ysics in the intermediate school." Pub-
lished by the Inst. Sci Res Inst of Pedagogical 3cienceo, Hin
Education Georgian 33R. Tbilisi, 1956.
(Dissertation ror the degree of Candidite in Fedago.~-iLcnl Jclencej)
SO: knizhnayu Letopis', i4o 36, 1.956, I.Ioscow.

S. CAPT
PA 18./ItOTA2
USSR/Medicine - Gonorrhea, Cure of May/Jun 48
Medicine - Turpentine
"Treatment for Sulfamide-Resistant Gonorrhea With
l0lebintin, Injections," Capt M. S. Namicheyshvill,
Me& BV) I p . I
"Vest Venerol i Dermatol" No 3
Describes successful treatment of sulfamide-
resistant gonorrhea using turpentine injectionB.
18/49T82

Author of articlet "The Prophylixis of Trauma of the Skin," giving advice
on the treatment of skin wounds. Sovetskaya Armiya, Group of Soviet Forces,
Germany, 4 Aug 54
Author of a letter to the editors of Sovetskaya ArmiZa complaining of the
inadequacy of propaganda on health and hygiene among the troops of the
Group of Soviet Forces, Germany. Sovetskaya Armlya, Group of Soviet
Forces,, Germany, 27 Aug 54
SOt SUM 291t 2 Doe 1954

M.-

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Vetariiiaariya; Vol. 31; io. 2; Fcbj-uary 1954 Uncl.
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ro 0 0 0 0 0 01810

AFELITSYN, I.E., doktor tekhn.nauk; BARS, Ye.A., kand.geol.-min.nauk;
3CRISOV, Yu.P., Imnd.tekhn.uauk; VELIKOVSKIT, A.S., prof.; TYSOTSKIY.
I.T., kand.geol.min.nauk; GOVOROVA, G.L., dote.; DAKHROV, Y.N., prof.
UDANOV, H.A*, prof*,- 7.HUKOV# A*L, dote.; KOTTAUOT.Y.I., prof.;
KREMS, A.Ya,. doktor geol.-min.nauk; MMIAVIYEV. 1.M., prof.;
HUSHIff, A.Z., inzh.; JUHIOT, A-Kh., k~nd.tekhn.aauk; KHODANOVICH,
I.Yee, kand.tekhnnauk; MLYSTOV, Y.T., inzh.; CHKRYOT, B.G., kand.
tekhn.nattk; SH(MOV, V.I., dots.: SAVINA. Z.A.. vedushchiy red.;
POLOSINA, A.S., tekhn.red.
Dfanual to petroleum extraction] Spravochnik po dobyche nefti.
Pod obsbehei red. I.M.Yuravlevs. Moskva. Goa. snuchno-tekhn.izd-vo
neft. i gorno-toplivnoi lit-ry. Vol. 1. 1958. 540 p. (MIRA 11:4)
(Petroleum industry)

AID P 2692
Subject USSRIKInIng
Card 1/2, Pub. 78 - 10/21
Author Namiot, A. Yu.
Title Change of temperature along the shaft of a producing
well
Periodical : Neft. khoz., 33, 5, 45-48, MY 1955
Abstract : The author analyses the drop in temperature of oil
when It in lifted in the well shaft. Such tem-
perature changes are dependent upon the drop in
pressure, the thermal conductivity of the media
crossed by the well shaft, the rate of the oil
discharge and the gas/oil rates. The proper
appraisal of the drop in temperature Is especially
important for paraffin oil wells when paraffin is
precipitated at lower temperature and forms a
deposit on the well piping.

15-57-7-10082
Translation from: Referativnyy zhurnal, Geologiya, 1957, Nr 7,
p 202 (USSR)
AUTHOR: Namiot, A. Yu.
TITLE: Temperature Ghange Along an Oil or Gas Drill Hole
(K voprosu ob izmenenii temperatury po stvolu
neftyanoy ili gazovoy skvazhiny)
PERIODICALt Tr. Vses. neftegaz. n.-i. in-t, 1956, Nr 8, PP 347-360
ABSTRACT: Bibliographic entry
Card 1/1

IUKLYEV, V. M. XAMIOT; A. Yu.; ~GIMAMA, M.M.; ULITANINSKIT, B.V.
Paraffin a posits from formation oils. Trudy MI no-8:369-
378 156. 7 (MLRA 9:12)
(P,aridfins) (Petroleum engineering)

1-7 ,a L,,--
USSR/Chemical Technology. Chemical Products and Their Application Treatment of
natural gases and petroleum. Motor fuels. Lubricants,
1-13
Abst Journal: Referat Zhur - Khimiya, No 2, 1957, 5496
Author: Mamuna, V. N., Grcmova, A. A., Namiot, A. Yu., Fokeyev, V. M.
Institution: All-Union Petroleum and Gas Scientific Research Institute
Title: Mutual Solubility of Carbon Dioxide and Rcmashkinakaya Petroleum
Original
Publication: Tr. Wes. neftegaz. n.-i. in-ta, 1956, 110 8, 392-399
Abstract: Investigation or mutual 1 bility 'of, C02 and Romashkinakaya petroleum
(molecular weight 253, d~g u-8736, content of paraffins 3.40, of tars
15-75% by volume, starts to boil at 600) under conditions correspond-
ing to the average stratum conditions of the Romashkinakoye oil field.
The C02 used was contained in cylinders under a pressure of 60 kg/cm2
and included