SCIENTIFIC ABSTRACT SHEVELEV, S.A. - SHEVELEVA, A.A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001549320001-6
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 9, 2001
• Sequence Number: 1
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

NOVIKOV., S.S.; SLOVETSKIY, V.I.; SHEVELEV, S.A.; FAYNZILIBERG, A.A.
Spectrophotometric determination of the dissociation constants
of aliphatic nitro compounds. Izv.AN SSSR Otd.khim.nauk no.4:
598-605 AP 162. (MIRA 15:4)
1. Institut organicbeskoy khimii im. N.D.Zel-inskogo AN SSSR.
(Nitro compounds) (Dissociation)

SLOVETSKIY, V.I.; SHEVELEV S.A.: YERASHKO, V.I.; FAYNZILIBERG, A.A.;
NOVIKOV, -
Structure of salts of 1,1-dinitroalkanes and trinitromethane.
Izv.AN SSSR.Otd.khim.nauk no.6:1126 162. (KRA 15:8)
1. Institut organicheskoy khimii im. N.D.Zelinskogo AN SSSR.
(Paraffins--Spectra)

S/062/63/000/001/007/025
B101/B186
AUTHORS: Slovetskiy, V. I., Yerashko, V. I.,
Paynzillberg, A. A., and Novikov, S. S.
TITLE. Spectrometric structural analysis of the salts of
1,1-dinitro alkanes and trinitro.methane
PERIODICAL: Akad'emiya nauk SSSR- Izvqstiya. Otdeleniye khimicheskikh
nauk, no. 1, 1963, 57-63
TM: A comparative study was made of the IR spectra of the lithium,
p6tassium sodiurn and aminonium salts of 1,1-dinitro methane, 1,1-dinitro
et.hane, 1,1-dinitro propane, 1,1-dinit-robutane, 1,1-dinitro pentane,
1,',1-dinitro hexane, 1,1-dinitrodecane, and trinitro methane, in order to
elucidate their structu"res. Results: All 1,1-dinitro alkanes hake bands
at -- 1450,-1210, and - 1120 cm-1, but no bands characterizing the
stretching vibrations of N-0 in the noncharged NO groups exist in the
2
spectra of any of the compounds. The spectra of the salts show neither
the two bands in the region of 800-900 cm-1 that are found in free gem-
dinitro alkanes, whereof at,fleast one is caused by the stretching vibra-.
Card 1/2

S/062/63/000/001/007/025
Spectrometric structural Bi-ol IB1 86
tions of the C-N bond, nor ~a nds characteristic: 'of the C-N bond. The
nature of the cation has no effect on the spectrum except that in ammonium.
salts additionally Mi+ - ion balids appear as well:,.as a weak 1580 cm-1 band
4
produced by hydrolyais, Cohclusion; All nitro groUDs are equivalent
and participate similarly ia.the formation of the,anion. Hence, the
F RC (.110 Mit and D(N02)
formulas of the salts are :-- 2)21 31 M No
carbanions are present. There-are 2 figures and'5 tables. The most
important -EnGlish-languaee 'references are: N. Jonathan, J. Moleoul-.--'
Spectra, 7, 105 (1961); L. Kissinger, H. E. Ungnade, J. Organ. Chem.,
25, 1471 (1960) .
ASSOCIATION: institut oreanicheskoy khimii Akademii nauk SSSR
(Institute'of Organic Chemistry of the Academy of
Sciences USSIR)
SUB:.:ITTi;D: March. 26, ig 62
Card 2/2

SHLYAPOCIMIKOVY V.A.~, _SH~,-S-A,~-YERASHKO, V.I.; FAMILIBERG, A.A.;
NOVIKOV, S.S.
Intensity of stretching 14-0 vibrations in nitro-alkst and halogenated
nitro alkanes. Izv.AN SSSR.Otd.khim.nauk no.9:1684-1686 S 162.
(MIRA 15:10)
1. Institut oganicheskoy khJmJJ ii. N.D.Zelinskogo AN SSSR.
(Paraffins-Spectra)

XOVMVP S.S.; BABIYLVSKIY, IVANOVAJ I.S.; YAYNZILIBEM, A.L.
~yntheeis of l,lvlv3,-tetranitro-2-a:Lkylpropanes and their cleavage
by the action of bases. Izv. All SSSR.Otd.khim.nauk no-10:1853-1855
0 162. (MIRA 15--10)
1. Institut organicheskoy kbimli im. N.D.Zelinakogo AN SSSR.
(Propane) (Ba'ses (Chemistry))

EOVIKOVY S.S.; SLOVEETSKIY, V.I.; TARTAKOVSKIY, V.A.; SHEVELEV, S.,~-;
Ftk~QIZIL I BERG, A.A.
On the existence of aci-forms of 1.1-dinitroalkanes and
trinitromethane. Dokl. AN SSSR. 146 no.1:104-106 S 162.
(MIRA lr:g)
1. Institut organicheskoy khimii im. N.D. Zel-inskogo AN SSSR.
Predstavleno akademikom M.I. Kabachnikom.
(Paraffins) (Nitro compounds)

SLOVETSKIY, V. I.; SHEVELEV, S. A.; YERASHKO, V. I.; FAYNZILIBERG., A. A.;
S. -S-I--..-"-,,-. . I .
NOVIKOVY
Structureof salts of 1,1-dinitroalkanes and trinitromethane
studied by spectral methods. Izv. AN SSSR. otd. khim. nauk
no.1:57-63 163. (MIRA 16:1)
1. Institut organicheskoy- khimii AN SSSR.
(Paraffins--Spectra)
(Nitro compounds-Spectra)

)ERAS I i!W, T. I. -.t ~541liT,14-FUl , S . k. ~ FA~ W' "I'Ll I BER :G, A. ~ ,
Ouair-an-limt prejeess of obtaining d--tuil-,r,~ ard
mflil.l.a.lo, --i*zr, AN kh-lit . -a: . 11.2060-41061 e 65.
(MIRA :L8tll)
I
.L. WimIL Lm. Zelirlsklogo AN, &;SR.

L 36505-66 E'-NT(M)/EWP(J)/T VFW/Jn/WE&-',
AtC NR, AP60J7880 SOURCE CODE: uR/oo62/66/000/005/0930/0932
AUTHORt Ustynyuk, L. A.;_Shavelev, S. A.; Faynzi-l'bergp A. A.
ORG: Institute of Organic Chomist.ML.Lrj.,. i demy Sciences, SSSR
(Institut organicheskoy kh!~R Akademii nauk SSSR)
TITLE? Effect of acylating agents on salts of 11,1-dinitroalkanesi
SOURM AN SSSR. Izvestiya. Soriya khir~icheskaya, no- 5,, 1966, 930-932
TOPIC TAGS: acylation, organic nitro cumpound, ethane, propane
ABSTRACT: The reactions of salts of gem-dinitroothane with the acylating agents
acetyl chloride, acetic anhydride, acetyl nitrate, U-enzoyl chloride, methyl chloroa-
cetate, and p-toluenesulfonyl chloride were all found to produce dinitroethyl at
trolate CH3C(NO2)=N--O-C(NO2)2CH3 (I). Its yield varied over a wide range with the
conditions of the reaction, i.e., the nature of the solvent and cation, proportion of
the reactants, and temperature. Thus, in the reaction of the potassium salt of gem-
dinitroo-Uhane with acetyl chloride inpolar solvents (acetoney acetonitrilet dime
formamide), the yield of (1) was - 30;4,, but in solvents of low polarity., where the
potassium salt is practically Insoluble, (I) was not formed at all. If however the
triethylamine salt of gem-dinitroethane, which is soluble in aU these solvents, is
introduced into the reaction, the formation of (I) in substantial quantities is always;-
UDC: 542.91 + 547.232

I
L 36-`05-66
~Cc NR:' ' AP'601?880
observed. The effect of acylating agents, particularly acetyl nitrate, on salts of
,- ane, 1,1-dinitropropane und
1,1-dinitropropane was also studied. Like 1,1-dinitroeth
these conditions was found to yield a product of autoxidation, dinitropropyl propyl-
nitrolate C2H5C(NO~Z)=N-OC(NO~)2C2H5.
SUB CODEt 07/ suam DATst o8oct65/ oRIG REFt 001/ OTH REFi 002
Cmd -_2/2

SLE"T - ,
.-.,Fr:-i7 S. B.
"Meetings of the Che7acal Sciences Section 28 - 29 Sentember and 26 - 27 October," Iz.
Ak. N`auk- SSSR, OtIdel. 'IhLlm. Nauk, '-,o. 2, I'The Comission on Scientific Photography
and Cinemato -ra-.-)hy, of the Deoartment of Chemicall Sciences of the AcaderrT of Sciences of
the USSR," icid., No. 6, 10,49; "General Assembly of the Department of Chemical Sciences
of 'he Acade-,~.q of Sciences of the USSR," ibid.

SHEVETU7-v - V-
--------
Improve the -'planning and utilization,of the working capital of
enterprises. Den.i kred. 17 no.4:25-30 Ap '59.
(MIRA 12:8)
(Finance)

SHEVELEV, V.
Bank control over the observance of an economy regime by enter-
prises. Den.i kred. 18 no-5:25-31 MY 160.
(MIM 13:5)
1. Upravl1rayushchiy Leningradskim otdeloniyam Gosbanka Mosk.V7.
(Moscow--Costs, Industrial) (Moscow--Banks and banking)

ZHADAN, V.Z.; SIMVELEV, V.A.
Automatic control of airtightness in sealing canned food. Kons. i
ov. prom. 14 no.10:15-19 0 t59. (NIRA 12:12)
1.Odesskiy- tekhnologicheakiy institut pishchevoy- i kholodillno7 pro-
myshlennosti (for Zhadan). 2.Odeaski7 mashinostroitellny7 zavod imen4-
Kalinina. (for Shevelev).
(Canning and preserving-Apparatus and supplies)
(Sealing (Technolog7)

~HEVELEV,-Ya-iliy-Alekaeyzyi.ch, BORULYA, A., red.; TELEGINA, T.,
tekhn. red.
[Bank control in induatz7]Bankovskii kontroll v pro-
myshlennosti; iz opyta raboty Leningradskogo otdeleniia
Gosbanka Moskvy. Moskva, Gosfinizdat, 1962, 73 P.
(MIRA 16:4)
(Moscow-Banks and banking)
(Moscow-Auditing and inspection)

TUROVA, A.D.; SHEVELSy ,4A.-;- BAN' KOVSKIY,
-- ---A _ A.I.; ALESHKINA, A.A.
----
New drug Ocardiovalen" for heart diseases. Apt.delo 5 no-3.-43-45
Mq-Je 156. (MIRA 9:8)
1. Iz Veesoyuznogo nauchno-issledovatellskogo instituta lakarstven-
njvkh i aromaticheskikh rasteniy (VIIAR)
(PHARMACOLOGY) (HRM--DISEASES)

SHBVM3V, V.A., kand.khimichaskikh nauk
New preparation from fresh medicinal plants is NPlautago juice.w
Apt.delo 8 no.6:1(0-7j,"k~TD 159. (MA 13:4)
1. Iz laboratoril tekhnologii Vsesoyuznogo nauchno-isoledu7atell-
skogo instituta lekarstveuuykh i aromaticheskikh rasteniy (VILAR).
(PTANAIN)

SHEVELEV) V.A.; BANIKOVSKIYq A.I.; ALESHKINA, Ya.Ae
Active substances of the cardiac drug "Kardiave4len.1 Trudy
VILAR no. U:317-329 159. (MIRA 14:2)
(CARDIAC QLYCOSIDES)

ROSTOTSKIY, B.K.; ,SHEVELEV9 V.A.1 BANIKOVSKIY, A.I.
Methods for obtaining an insecticide preparation from Anabasis,
Trudy VILAR no. 11:330-350 '59. (MIRA 14:2)
(AILUMSIS (BOTANY)) (ALKAWIDS) (INaCTICIDES)

SHEVELEV, V.A.; BANIKOVSKIYv A.I.; MURAVIYEVAy V.I.
Q- ---
Machine-drying of opium raw material.. Trudy VILAR no. 1-1:351-353
159. (MIRA 14:2)
(BIOLOGICAL PRODUCTS-DhYING) (OPIUM)

BANIKOVSKIY, A.I.; PERELISON, Me.; SHEVELEV, V.A.
Alkaloids from globe thistle. Dok1. AN SSSR 148 no.5:1073-1076
F 163. (MIRA-16:3)
1. Vsesoy-uznTy institut lekarstvennykh i aromaticheskikh rasteniy.
Predstavleno akademikom M.M.Shemyakinym.
(Echinopsins)

SHEVELEV, V,.,',, KREVUT, B,Azj KILSELEVA, Ye,Ya.
Analyala of pharmaceutical preparations by the capillary
fluorescence method. Apt. delo 14 no.5356-60 S-0 165.
(MIRA 18311)
1. Vsesoyuznyy nauchno-issledovatellskiy institut lekarstvennykh
I aromatiches~akh rasteniy, Bittsa, Moskovskoy oblast.i.

(Y)
260)
IMOR31 Dxitroch.nkoo D. A- Lcb.ncw, A. W.,

TITW Appaza 1"o f:r K-ouri.jt Dt.14ctri. LQ..o. and %h- t-re--hility
0t Solid DI I.Q%rL 0.
PZRICDZCALt Zovodskay. 10orstorlya, 1959, Vol 25, Ir 9, FP 1121-1124(0531)
AISTRACT I The "Cleo of dielectric loan** Ig 6 atd the dLelootria
4 elect I within the rands of declacter waves art at present
1
,
ng ao4sur.d according to two zotbo4* - 1) of the coaxial
11:
1
ILA.. 2) or the coaxial resonator (CA) ( 11, to 1-5). 7h v.Llabl.
tractions at (CA) do not, h ... war. &I," me uxt t
a wide temperature ravSe. A (CI) has b..m
1b It, a values h
so. The br...
t1do 4% 0 a
Mb.r 1::;.r
;*4 I 1Ag oold.r.4 with
th, lon:r
qyiind.r sib 1.0 Govor:,
:
r. The eupport.
.
.
@liver to the inner a 14 f be I . on r
604 G*".Otiag tube# of sho (CA) to the Con rattr Ad

T
"
on ' a a
opposite each other h Id. -4
1,:
11:t

..
~
Tbv
.1
h .
a*1 f the C war I.,. w*4
4
r
p
or
11
!
6500 1'h %h r
tz.4
1
.
4-fa0t., of 1, RR~ :
:*
.Yet
factor of 10$000. Froa the blook itagram of he a
Card 1/2 r1jg 2) 1% own U. seen %he t %h. (CR) 1. connect ad via art &b-
:GrPtl OR-Attoaualor (.ilh on - 20 4.clb.10) to &
.a.r4lw of tYP- 033-12 (frvq.eacy r.m,. 160~0000 m.C.aycl,s).
MPIMOT 20.1M to used 49 lad:44tor. T-~porsturs was
in am olz..djr d-tcrlb*d -$hod (j.t
'he 141U.8 It 6
r::M!
It oncarnins the %-mler Ir.
function of thu.
T"u**' "I' red from sampl.s of oll
n4 pol %rat Nor. . .,. r be
quart %hYl-n- (?it 3), "a to
re.ults how the$ the describe d d*t.rai.attom method I- -ulk.bl.
for the examination of polymer dielectric&, in which tC a
.. of 10,2.
There are 3 f1cr.0 and 10
r of which are Soviet.
ASSOCIATION9 149tit-t 17sOkOm.l.ku1y.rnykh 0-7-dLA-4iY AkAde.14 nA.k azialt
(10:tlt o.for)HICh Mol-lar Cmp*uAjg of 14
3 :t A0.4.4y at
at BAR
Card 2/2

YWE I IrJ)!. UMITATIGfi SOV/4379
kon!"r-tey. po flake di.l4'xtr1x- 2d, 19513
Fisiks Jjelsktrlk~; tradjr vtoroy voosyusnoy koftforectsil (Physics of Dielo-tric.,
Ir.,w tiOo* of %b. 2d kll-U:ao. CoOf.r.~.. an the Physic. of DI.je.t:t-j
moscm, lad -0 AS S= , IVO. 532 p. Errata slip insert*4. 5,000 copies
printed.
S"rearine ke-Urf Ak.40214. cauk =P. 11101bo.kly lostitut I .. I P.11.
Ed. or Pubi-IWI.g Hous.. T..L. St.r.k.d--kay,, Tech. Ed., I.N. Darcithin.; Edi-
tortal BOArd- ~R.op. Ed.) C.I. Sk.-I. Doctor of Physics -4 F.th-tic.
..d X.7. 1111ppl., C.ndil.te of Physics and
MItME, This call-tic. of rep~.ts 1, i.t.rvled for ei-tists
the physits of dielectrics.
COVERAGE1 The 3-toni L11-Umion. Co:mfersm- to the Phlvt~.l of Dielectrics bold I.
Kw- at th. Fi,iib.skly i-titut I .. I P~9. Lt-d-a (Pbyst,s institute i-.i
P.N. Lbod.v) 1. no,-b.r 1959 ..a tt4.--J-d by r.p-mt.ti-s of the p,i-1p.1
sciont4fic sent*-, or tho U&il &M of several cth4 r c o-tri.s. This ccl-
1-tim catlm. wat of the reports presented at the conference " -rigs
of the dloc"alon, hich f.11cd. Th4 r.,~,t. in thil d-1 Jth
dielectric properties, 118,01, and P-1-Itstion, sal ~Jth p~cjfjc iod~ctj,.
capacitance of '~i... crystals, eh~acl c,--p-dm, and c.r"jc9. Phot-
9lactreti, crystal., sol v%rjo~uj rallstiao and Irre.4ialuun *f-
foots an d.14lectrl:s are iArest-&ated. The T51=0 cc~talnl 4 list of othpr
p p-re ppoafnt-4 at the conforenco dealing with ;,laritnticm, losses, and
C
remkcimns of dieleltrics, vh1ch were publIshta in the jcuc~t&j IsT*.tijra AM
SM..eril. fIzIth-k-T-,?4- I d~ "W.. 01 p-t-lilies s,, aeAticad.
RoN .aA-C.&Tany each rip-r.
X.Te. LIjk*r, andjjP-_fS'A~L~Teapvr%t=o Dopemiento
~Tfl`iof Certain 21
ladacti't c4p.-I...mo and Losses of so..
""'I""ney Alectr-Ic fields at Hl;h Te=porstwre
[Sibirskly fitiko-tokhaich.skly 11.1, T-1-- tSAbtrla. Physics ad Technical
Saiantifig: R.1.8~h Institute, T-k)] 2A
Disc.04too 37
I I the St4t", Spe,,ific Inductive Capacitance
UjLD.k2t,LJ~ On the Pmblm a.
__
of H#t*mg*z"us D141fttrics [voro' gsbokiy moVakcabilyaystyeanyy institut
(Uroz.th kgrialtwal lost Itut.)] 39
Ar 941;211. 1.7. Dielectric Parameters Of Double Liquid Syst- In the
'lc. L-rco... A,---1 1 1.9
DijF4.-11on ~bv.",j in 3-4 D!-I"trics at AU4
1.
1
React Voram.sh Agricultural Inititutel
57
Perna,, I..x., m L.',-dj~n
-DIA-tric Prorertles Of Boltro
-cus
e
65
Disc-..ion
77
and A.
Y. L-b-". st-Al a., E, ",i t'b I
or
rualt- - of at Igh Fr qu*rA-,., I'k.1-
YA=Ykb 1'1~-Ift-uljr AM =R~ Leningrad (Institute z, Hig,
C-Pounds
A3
,
U= , L-Atfred)] 91
Br-in S M,Dlelettrii CL&r.ct.r1.tjj9 (C acd tO ) of Impr#rmstpd Cable
z O.r in RAIAti:n to th- Prc;*rtIrj of the
(Fftper
E,,
,
I....it,t 0'-c- F-r Fni:1-rin; j-,.jtutj)] 9-1

105
the Dj---'., Th-, of 'berOil I.
1r .... D-, and On the
-
mov~mt of D1 1,44-rc
A To !1:1i'ltrot-tnich,okly
ia.titut I.. Y.i. n,y",,. (L_jn,.d Elactrat'J~ic.l :~~tltutt
izent V.I.-n1y-,, (1-~iafl 124
Dmitroch-ko D-1-, and V.A. S"IeTolev. U14 of C-timl Hoso~toro Far
-
I~Z6 -- _i'
j,.dwtj,. C.p.:L._. in
-
~Ift3titut9 of H1gt Molecular C:rounda, Ac%doay or
132
Zb~lud- I-S- ~d Pho'.001-tl.t. -d On.
~
-
-
't kiist
-lloC--fl
i
IX 555"L Y~d:- of Cri.t,l-
A-A.:cy of 511'a-, USCR, Mo-))
G,bkta. A.H. sod Charge St.bilil
a, lriorC-lc 11.ct~'tm
-t 11 -AA it I t .! 4- P.M. A.-, UjR: K-C"
l

MIKHAYLOV, G.P.; IOBANO~, A.M.; SHEVELEV, V.A.
Temperature dependence of the dipole-elastic relaxELtion time of
polymers. Vysokom.soede 3 noo5.-794-797 Hy 161. (KERA 14:5)
1. Institut, vysokomoleku-1yarnykh soyedineniy AN S SSR.
(Polymers)
t,

S/032/62/028/002/028/037
B120101
AUTHD"16: inikniaylov, G. IF., Shevelev,_V. A.-, and Dmitrochenko, D.
TITLE: Device for measuring dielectric losses and dielectric
constant of solid polymer dielectrics
PEz?101)ICiiL: Zavodskaya laboratoriya, v. 28, no. 2, 1962, 234-236
TEXT: El and tand can be measured in a wide temperature range with a
Setup based on the -standard measurii.g device. The measuring circuit was
connected with the s~andard-signal generator FCC-17 (GSS-17) tnrough
attenuator Al-I (A3-1) and yp-1A (UR-1A) or YP-2 (UR-2) broad-band
am,;lifier. The measurin7 amplifier 28gM (28IJ%) was used as resonance
indicator. The resonance frequency was checked with a YBP- (UVR)
wavemeti_,r. The first modification of the measuring circuit, shown in
Fig. 1,a, is designed -'or use in a .,iide temperature range. The dielectric
sample is placed into the -ap of measuring capacitor 2 containing no
mobile electrodes. Insulation 3 is made of a high-frequency oeramic
material. Thermostat 5 ensures constant temperature of loop 6, induction
Coil 7
,, detector crystal 6, and screen 9. The second modification, shown
Card 1/4

M
S/032/62/028/002/028/037
Device for mea6uring dielectric losses ... B124/B101
in Pig. 1,~, i5 designed for measurements at room temperature, with
trimming condenser 10 being as close as possible to the gap of the
measuring capacitor, thereby permitting accurate measurement of the sample
capacitance. Plane parallel sample disks with a thickness of 0.001 to
0.005 mm in excess of that of the gap between the electrodes were used ,
the diameter of which was calculated from DO'