SCIENTIFIC ABSTRACT ALEKSEYEVA, V. - ALEKSEYEVA, YE.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000101010010-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 24, 2001
• Sequence Number: 10
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

_ MUIT:NA, L.D.
1, MV'~A;,YA, II.D., kund.rmd.."uk; dXKSEY~VA, V.G,;
Adio avMrom. Ve*rt. derlr,. I von. )S no.~1:71-73 5 1~4. (MI RA 113:4)
1. j.4jrij,ngm'rl*riya dt tl,llr"lsu (f,'Irtvnyy vrach
S.I.OxcidskiT).

L
ACC NR: AP6010700' SOURCE CODE: UR/0106/66JO00/002/0056/0066
,AUTHOR: Aleksayeva, V. 0.
ORG: nom~"--- ...... ..
TITLE: ;Phase distortion in transmission systems and "image" characteristics of,
!!JL ~ai a
SOURCE: L1ektrqisvyaz', no. 2, 1966, 56-66
TOPIC TAGS: trainamission system, signal tranernission, pbase distortion
ABSTRACT: It hahs been repeated.1y pointed out that a gyrninctrical pulse loses its
symmetry when phase distortion occurs. This article attcmi,lf, to explore the
causes or disruptunn of "irnage" characteriatics of signals; each function F'(t) and.
F"(0 in an "Lmage" of 1he other If F'(0 . F"(-t) and F-1-0 . F"(0. The system
response to the appli cation (cessation) of a unit step voltage i.-.i called turn-on
(turn-off) function. K-clijanons are set up and investigated which describe a system,
with ideal phase characteristic, a I-f syntern with phase distortion, and a hand-
pass systern with phase distortion. Experimental data on a multiplexing single-
repeater chaLnnel publislied elsewhere in compared with aome data estimated from
Card 1/2 UVC: 621.391.833.2

L 35909-66
ACC NR: AP6010790
the theorT developed in this article. Theme conclusions are offered re transients
accompanying the application and cessation -of symmetrical pulses: (1) At the out-:,
put of an ideal-phuse-frequency-characteriatic 1-f system, the turn-on and turn-
off functions have "image" characteristics; the pulses preserve their symmetry;
(2) At the output of a phase -distorting system, the above functions lose their
"image" characteristics; pulses become asymmetrical; (3) At the output of a
band-pass filter having an ideal phase frequency characteristic, the turn-on and
turn-off function envelopes are "images, " but are connected by nonlinear
relations; the pulses are symmetrical; (4) At the output of a band-pass system
having arbitrary phase distortion, the envelopes are not "images" and are
connected by nonlinear relaUans; the pulses are anymmetricali (5) A two-band
transmission of signals over a system having even curves of amplitude and phase
distortions to an exception to the general mle of determining phase distortion by
the disruption of symmetrical properties. Orig. art. has* 7 figures and
30 fortnulAmi.
SUB CODE- 09 SU13M DATEt ZSM&y6S ORIG REV: 004 1 OTH REF: OOZ
Gard z1z..,eAq-

^CC N"I AP60331587 SOURCE CODES UR/OiBi/66/008/010/3138/3140-
AUTHOR& Alekuey~va, V. 0. , Landeberg, To. G.
Of4l InatituU of MWIa Engineering and glectroaLe AN &MR. Moscov (Institut
rsaotel-baLki I clektnmiki AN SSSR)
TITLE: Certa.La electric and photcelectric properties of the compound SWI
SOURCE: Milt& tvardago tGlIL, V. 8, no. io. 1966, 3138-3140
7WIC TAGS: antimany coupound. photoelectric property, sexiconductor single crystal,
ferroelectricity. resistivity, activation energyv Hall effect, electron mobility,
absorption bond
AIISTRAM -,he aUthoLrm have investigated the electric and photoelectric properties or
single crystals of SWI in the Verroelectric region. Small amounts of Lil were in-
troduced into aoine of the single crystals. The temperature dependence of the resis-
tivity was waijured in the 15 - 40C range. The resistivity decreased exponentia3ly
with incressinC teapersiture, vitb an activation energy close to that obtained by J.
Sasaki (Japan T. Appl. 'i-bya. v. 4, na, 1965 and earlier). The carrier mobility could-
U-t determined from %be Hall effect only for lithLum-doped crystals and amounted to
50 - 100 czzfv-aec. 1139 sign of the Hall ear corresponded to a-type conductivity.
Tae photocon4uativity of 11thiura doped crystals, measured after prolonged storage in

A C MR. AP6033567
darkness, was 10 - 20 times larger than that of the pure samples. Both samples showedi
sneering or use long-umve edge or the absorption band and a rap!d decrease in the
photocurrent In the o1wrt-wave side correspooding to the intrinsic absorption. 7he
low sbort-wava saftsitIvity is attributed to surface recombination. The decrease in
phot,ocoaducti-rity ban a complicated character. Measurements of the thermally stimilt.
lated conductivity d1s,closed the presence of adhesion centers, but they vere unstable
and disappeared umder the Lufluence of light or heating. The experimental results am
izt.arpreted. frota the point of view that both doped and undoped samples contained two
types of doefecta, stale and unstable, and the letter am strongly affected by illumiw
nation. The at;Uors thank S. G. Kalashnikoy for a discussion of the results. Orig.
art. bass 2 figures.
6t3 COMs 201 GUBK LUM 12H&r"/ ORIG HEFt 001/ OTH REF: 004
2/2

A= M24 ARS035901 SOURCE CODE: UR/0274/66/000/008/A011/A011
AUTHOR: Aloksiyeva, V. G.
TITLE: The off of nonuatformity in the amplitude spectrum of a signal and the
transmission coelflicient of the signal compression circuit on the shape of the output
6~gnal
ISOURCE: Ref. zh. Radlotekhnika I elektroavyazl, Abs. BA71
REF SOURCE: Tr. Leningr. in-t aviats. priborostr.. vyp. 45, 1965. 38-48
TOPIC TAGS: appctrum, radio signal, frequency modulation, filter, amplitude,
signal amplitude,; output signal
ABSTRACT: The'effect of a deviation from the constant value of the product of the
spectral density of sin excitation signal with a linear frequency modulation on the
transmission coefficient of a filter with a rectangular frequency characteristic and a
quadratic phase dispersion was Investigated. It is shown that it leads primarily to arc-
increase in the mintmusn spacings separating two adjacent iterative signals. [Traim-
lation of abstractl INTI
BUD CODE: 171
Cd UDC: 621.391.14

KORIK KII MESEUVt I GOVOROVA H.S.; VOROMNA, T.V.;
11 )~ 40.
VA, S.14 "idZANTSEVA, G.V.; MOROZ, V.M.;
bulmok, A.S.; FIVINIYAN, P.061 MUMMA, A.K.
R
q
Trace elements in drinkifig water sources of Kazakhstan and their
relz toes to the problem of some noninfectious diseases. Vest. AMN
ssqy,~ n0.7:90-4- 164. (MlRA 18:3)
kllta-Ainskiy neditainskiy inatitut.

ALESSIMEVA, V.I., starably LmLb.
Track patrol. Put' i put.khou. 5 mo.10:25 0 161. (MIPA 14:10)
1. Poromyokaya distantsiya JUShno-SakhalirAkoy dorogi.
(Railroads.-Track)

AT EMA, r.1.0 kand.sed.vauk
.. .. .....I......... 1. .
Chalcosis of the eye =A its treatment by negative ionization.
Vest.oft. no.4tl3-18 162. (MRA 15:11)
1. Gamuls"tvexWy nsuabno-Iseledavatellskiy inatitut glaznykb
bolaxn*7 Imni Ool9mgcl*tsa.
(BYS-DISEASES MD IS) (COPM n TER BODY)
(MMMOMMIS)

ALEKWKVA, Vora lv&uovnaj VAY)ISHTEYII, Ye.S., re-i.
(Clalixomis of the eye] Xh&llkoz glaza. Yoskya, Medi-
tsina) '1965. 113 p. (141RA IS: r)

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I ;. :),%;"3.6, on tlv,
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Spectral of Scandium In Orf~s ---
AMCCIATION: MosnOw
S U EM I 11M)
Card

IVAWV4(IHOSIATTUV, Potr Ivanovich; WDORff, F.A.9 red.; ALSKSEMAt V.M.p
red.1 P=ff, G.P., tokbn. red. -
CUR brambes of the Cbmabbian industry] Navy* otrosli promwehleD-
momtl CkmvaWi. Choboksary, CbavaabakDo gos. izd-vo, 1960. 39 .
(KM& 34:7T
(Chuvashia-lbdustrios)

HUSA1101. A.K.; ATJMMA. T.K.-. KRITROT. T.G.-. KATIS. T.I., red.isd-va;
BMWVL, T.V.," tikhi.iid. *
[quantitative spectral determination of rare and scattered
elements In ores ana minerals) Zollobostvannye spaktrallnoo
op3nidalenls redicikh I resselanAfth alawntov v rudakh I stine-
ralakh. Noakra, Gos.nauchno-takhn.lid-vo lit-ry po goologli
I o1thrane nedr. 1960. 194 p. (91BA 13:11)
(Hotels, Rare and u1nor)

ALMISCMA, Y.M.3 MUCHMA, Ye.A.1 MYACIKCV, V.A.
. .....
Effoct of different surface active agents an the dearation of
viscoss and defoaming of a spinning bath. Khim.volak. no-3:30-33
161.
(KERA 14: 6)
1
1. V308oklirQ7 nauchno-isslodavatellekly Institut staklyanogo
volokna.
(Surface active agents)
(viscose)

5/075/62/017/007/001/006
B119/B186
AUTHORSt Ruilanov, A. K.# Alekseyeva. V. M., Illyasoys, N. V., and
Xhktrov, V. G.
TITL3t SpactrograpLic quantitative determination of small concentra-
tions of rare earths in rocks and minerals
PERIODICAL% Zhurnal analitichaskoy khimli, v. 17, no. 7, 1962p' 609 - 619
TEM A direct simultaneous determination of rare earths in ores was made
using a -15 (DYS-i5) diffraction spectrograph having a dispersion of
4 - 2 I/ma. Tho spectrum was excited by evaporating the powder sample,
mixed with buffer-mLiture, in a carbon are discharge. Otherwise. the
procedure followed the traditional spectrokraphic method. The standaird
oxperiven4al error of the method is 15%. The sensitivity of determination
is 0.00116 V*r Tb, 0.00% for Tu and To 0.005% for La, 0.01% for Nd, 0.03~6
'for Pro Gd, Dy, and Lu, 0.04% for Cet 0.05% for Sao Bu, Tb, Be, and Er.
The sensitivity CUM be increased to the 30 - 100 times by a simple chemical
enrichment of the samplon with rare earths. In the original paper the
analytic sptatrun lines of the rare earths and of the disturbing elements
Card 1/2

S/075/62/Oi7/007/001/006
Spectrographic quantitnzive deteraination... B119/Bi86
wero tabulsted Ott 5 paBes. There are 5 figures and 4 tables. The most
important Englisli-languago reference ist J. A. Norris, C. E. Repper,
An&lyt. Chem. 2.41, 1599 (19520-
ASSOCILT103i Vaesoy-umnyy nauchno-iseledovateltakiy institut minerallnogo
syrlytt, 11oskv& (All-Union Scientific Research Institute of
Mineral Raw Materials, Moscow)
SUBMITT10i Decomber 30, 1961
Card

Mikg, V.D~I~j ALEXWMA, V.M.,l A.S.
Emict .is hea% *~:rsatvmnt on the prcrert~'ss of pnly-einyl ohlor!dft
filmird~. Khl.m.' volok. no.Z%12..15 1615. (MIRA !P16",

AUR~IETIXA, V. N..
2CIIii ALEFIEUVA, V. F. Tralticheskiye zaryatiya ;o ~'iziolcCii .
Eatastvcznmnl3,e v shkolo, 1q49, No. 3, a. 8,"-W
SO: InClIS ~-IATEY, lol, 27, Moskva, 191.9.

,41 I;< Vdtjf':OV, i : 'kf -
AU=MYBVA. T.M.
..........
crobective role of fatty matter in radiation Injury of calls [with
RuVIerY in IndlAshl- Bi0fisike 3 no,l*-101-107 '58- (%IRA 11-.2)
1. Inslitut biologlcheakcy fisiki All SSSR. Moskva.
(ROLATION-4PHTSIOWGICAL XFMT) (FAT) (TXAST)

-A0,,,Twm*v, date.
~,A=Sxm
prg,WT&tlon of Ilona uarrov extract had its influence on the body in
raillation sickmems. Akt.vop.porel.trovi no.6:L44-89 1,;8.
(MM 13 '. 1)
1. Radidbiologicheskayn lalboratoriya laningradskogo institute pereli-
T"iya krovi (say. laboratoriyey - starshiy nauchnyy sotrudnik O.M.
Nmrav Oyer).
(?I$Wl 3VIAMS) (RADICION SICMSS)

On a*-caned lipophanarosis oboorvable in irmdiated colls. Zhur.
ob. bd.ol. 22 no.2$146-149 Vz"p '61. (MIRA, 14: 5)
1. 1"titut biofisiki AN SSSR.
(FAT) (YFAST) (ROUTION-PHYSIOU)GIGAL EMCT)

H.N.j MIDVEDEVA, G.A.; AUMSMA, V.H.
DwOmation of live, injured and dead micro-organism. Hikrobiologila
30 no.5tS55-62 3-0 t6l. (MMA 14t12)
1. Imstitut m1kroblologii AN SSSR L Institut biofiziki AN SSSR.
(HICHO-ORGUISM)

AT, EMA, V. NL
Dissurtatigm defended at the Institute of Microbiology for the aoademic
dogres of CWalidato of Blologioal Solducess
*Patty audLipoid Cel'Imlm Substancesi Their Condition and Sjgnificance
Upon PAdUtion &posws."
Vmstmft Akmd Hauk No. 4, 1963, pp. W-145

34757
S/020/62/142/003/025/027
B1441BI01
A=4DRS: M.* and Veysell, M. N., Correoponling Member
VSSR
'I ITLE: Imnartance of intracellular fat reserves for cell reactivation
after rakliation injuries
7ERIOD iCAL : Alt-&Jemiya nauk SSSR. DoIclady, v. 142, n-). 3, 1)62, 699-701
TEXT: Cell rea~^tivation after ultraviolet and ionizing irradiations is
depende.-A on i) tharacter of radiation injuries, 2) state of cell activity,
3rd 5) cell. atr%icture and function. This paper is a detailed study of the
third factor, p4irticularly of the regulating effect of intracellular fat
reserves. The variation of nutrient media by additions of saccharose
.And Ozlyrocoll Io obtain yeast cello rich in fats and lipoids and the
subsequent effecl an oxidation processes and radioresistance in irradiated
cells h-ave been doncribed previously (Biofizika, 1, no. 1, 101 (1958)~
In %he -prevent tentst the total content of fats and lipoids determined
in 48 hr culturair of Endomyces magnuaii (EM) by extraction with sulfuric
ether 3AU 11.11
Csir6 J/5') ?1,4 (dry weiftht) on a suitable nutrient Mediur- as compared

S/020162/1 4 2/003/02 5/02 7
Imnortance of intracellular fat ... B144/B101
to 2.214 on -insultable media. Celle were correspondingly termed as rich
and poor in fikt. 2% suspensions of both types were irradiated in 41
flyni-M 1'r,7111-30) x-ray apnaratus (210 kw, 11) ins, 3760 r/mill, without
filter,,, FM were irradiated with 150 and 250 kr uni Saccharomyces vini
with I'D,) 1(r. CnI13 anA controls were subcultured in Petri dishes with
ararize.1 beer wort ,mneJiatdy after irradiation and kept 6 - ) days at
28DC as 0.2 - O..02,:~, suanonsions in sterile tai, water aith daily
sutcultarini, in mart aear dishes. Reactivation was judged from the
percenlagv of c,:oloniea (colonies in nonirradiated controls - 100"). It has
been fount that EM cells rich in fat have much hither reactivati'on levels
and radiaresistnnres ~Fif.. 1). The state of the fat inc-Liviona %as
atuAled in, luminescent light in cells treated with aqueous solution of Nile
Ij 1 u e .Th-t antr4tcvIlular fat proved to be utilized in the process of cel'
react ivation. The present studios confirm increa-ied relic t ivat ion in
cello ricti Ln fa,te and prove that their react ivat i or. 'level _s much
-:iarticulurlly in the first 24 hr. There are 2 fi,fkirez and 8
raference!i: 0 Soviet mni 2 non-Soviet. The reference to the English-
lar.roa,,e -nu~,Iicttt.ion reats as follo*s: W. A. Pratt, W. S. M. Eden,
J. Nzt.. Cancer Inut., 15, 4, 1059
Carl P"',

S/020/62/142/005/025/027
Importance of intracellular fat ... B144/D101
ASSOCIATION: Inatitut mikrobiologii Akademii nauk SSSR (Institute of
Microbiology of the Academy of Sciences USSR). Inatitut
'biologichookoy fiziki Akademii nauk SSSR (Institute of
biophysics of the Academy of Sciences USSR)
SUBVITTED: October 3, 1961
Fig. 1. Reactivation of EM cello after irradiation with 150 kr (A) and
250 kr (6).
Legend: (1) colls rich in fato (11~ cells voor in fat& (a) vercentage of
cell surrivalml (b) days. 80-
ISO-
30.
Fig.
3100
ju
Card 3/3

Apmsrm L - -
.z ~ v m
Fu t 0'1 ig-lilr-c, H, Comj,:%nento cf D?-Ilr-, Their C,:~ndltfon nrid Sign-IfIcance
Duri-.9, FoLd.1,11tIon."
Irm-11rAtIon ul* iuniml and yearm cel]5 pr(Auct-o ct*,arg,-.~:; lr t,t,,. luminescfnce 11pids
and Incr-au'ur. the flmkntity of ;,-,roxidcr, and fatty aeldr. The nbo--nce of fatty and
Lip~:I(I r,-:-,ervt!s exortn a reguLating Influence on the Intens,ty of :xrdative processes
In thi., C~.,!-I and Inorq-uses Its radintion stability 11Y 30%
amadidikto dis"rt4tice Usted in M"I"jqg no- 7, 1964. The
Me rediolqUyal
Ortlelt did MOt SlAtt 4P*CIf%QMUq Mat degree %me ;V-&;=' . The amwftted
title* deal wIth studies w ndleticm pbWoIW, radiation blodoxistry,
*06ined tmumo and The influence or 1"latlam an regeowntIve proafteen,
TudUtIon uIwm*Iolqpr and UmmmicSy, mvA sudiation pbmrmeolqW.

I. To. Olockva, Inningradokly prospekt, 75-a, kv.56);
PIMMITUN, H.I.; ATJ=L=A, VJI.; GARGOLOYIL., II.C.; GOPMIOVA,
Y*JI.; IOFFE, F.M.; M=M, F.I.
Significance of owlvmd trentment In the effectiveness of
enirgical interventions in pulmonary tuberculosis. Vest. khir.
92 mo.4s28-32 AP 164 (,"IRA 18o1)
1. 12 kafedry tuberizuleza MentrallnoGo Instituta usoverahan-
wtvvvanlya vracbey (rektor - M.D. Korrigina) bollnitsy Mi-
nistorstva putey soobshchaniya (glavnyy vrach - A.A.Potsube-
yorko) I klinicheskoy boltnitsy "Zakharlino" (glavny7 vrach
V.P.Petrik).

KA41RU', 10.1i.; AIJ:r~SEYEVA, V.H.j 11MM, V.G.
Awt:MIOIC cal.cu.tatIm ct rd=ro-c~jfa,~-ts. ~akrobiol~gita
3"1 Jm-F 165. %MMA '18:7)
1. :Inll*,Itu.t blatogicherkoy fizIki All SSSR.

T-VII. VOI. ; 0i "C";Kj Y, ~,. 11.
of thi- mcirphology of id.:r7,Org&nDqms by asing autcmut-4c
-It',I,IYIIRr fO.- 'dCrOOblertel. 10 nc.3-.4163-469 165.
(mw 12111)
1. ~ttm'At--,t flzikl AN Moskva. Subritted
T
,' nn.

Tv%F-;Kc'1TLTA, V.M.; KAYINIR, II.S.
FI-tiorometrIc method of datarnirdng the anount of llipidB
in yetot calls. TSItologila 7 no.6t7?6-779 N-P 165.
(KIRA 39:1)
1. Luburatorlya biof'lzikl zhivykh struktur Inst-ituta b1ologicheakoy
fi-AAVI AN S!~.")R, Moskva. Subnittf~d -September 1964.

'ACC 'W- 0281%, -rA -) -S -0 6 =-- -SC O--DES1 -R-/-OO3-2/66-/-0-3-2/0-06-/-0-6-9-6-/0-70-0-:
HORS Rusanov, A0. LI-4 ca 3:11yasovat No V,
RL
i AU-Union Salontifia Researob Thatitute.for Mineral Raw Materials (Vaesoyu&nyy
-hno-issledovatellskiy institut minerallnogo cyrlya)
Minination of the mtual affoot of tantalum and nioblum in the speotrum
ii or minerml area
: Zavodnkaya laboratorlya. To 32, no. 6. 1966. 696-700
TOPIC TAG3i spectrum analysis, tantalum. niobium cobalt compound
ABLSTRACTr 1ho article proposes a spectral method for stimultaneous determination of
niobium and tant.&Ium, which eliminat03 the mutual effect of these two elements. The
nethod As bdswl mi the addition of cobalt chloride to tho samples being analyzed. In
the intonal. the reproducibility (variation coefficient) of a single
detormination of tantalum and nioblum is 11%. it was found that the effeet of niobium
on the intensity of the tantalum lines can be eliminated by the creation of conditions
under which tant&lum will appear In the are cloud Independently of the &PPOArance of
nichium. Mtis is aahisvod by the addition to the samples of reagents (metal chlorides
or fluoritiai) %bloh lead to the formation of new compounds. 7he experimental results
givan in th4 article were obtained by additions of anhydrous cobalt chloride. It
.Ccw.d - I -UDC:__543.42-

f-ACC Nits--.
"28192
fol.low frogn the (jaj4j that both tantalia and niobium can bH& determined by this method
in spits of the presence of up'to 2% nibbim in silAcate area. It was fow-A that
considerabU chamgee in ooncentration of twwgetan. sirconlum, and thorium In the
mmples do not Wsct the Intensity of the niabium lines. Orig. art. hams 6 figures
2 tablen.
COM 07. 111 SM DAM uome/ MM RM 004

US PIYAMWA, ~LD.j SUMANBU, R.114%.
Albumim-urea-formMehyde glue for particle boruls. Der.prcm. 10
zk*m5s20 X 161. (MIRA Us 5)
fGlus) (Mutbmue)

Inv

r

OL
pr
JQ F

8048S
S/020/60/132/62/32/067
3 YJ 49 B011JB002
LUTHORSs r6orsbikk. V. V. corresponding 11ember AS USSR, Sosin, S. L.,
Aloksoyeva, V. P.
TITLEt The Production of Now Types of Linear Polymeralby Means of the
leaction of Polyrecombination
PERIODICILs boklady kkademit nauk SSSR, 196o, vol. 132. No. 2, pp. 360-363
T=Ts The authors treated dlphomylmethano, some of Its derivatives, methyl
enter of pbonyl sootto acid, and tensyl bentoato with tertiary butylperoxide
(1.2 and more moles per I mole of the initial substances) at 2000, according to
the methods desorIlied in Rof. 2. Thus they obtained polymers containing no
noticeable amounts of tridimensional structures. In such cases hitherto it was
only possilble to obtain dimore (Refs. 3, 10). Now a linear polymer was obtained
from diphsay1methave which the authors consider to be a polydiphonylmethylons (I)
and which hitherto has not been known (so Scheme). It is a yellowish powder
soluble In benzene, with a melting point :f 205-2200. Its molecular weight
varies between 10000 and 900000, according to the molar ratio between peroxide
and bodrociLrbon. Against all expectations, this polymer shows no inclination
Card 1/3

8046.5
The Production of NOW Types of Linear Polymers by Means S/020&/132/02/32/067
of the Reaction of Polyrocambination S011/ .0,02
to decompose into free radicals in the presence of diphenylpicry1hydrazine. It
is also largely stable towards HIM and chromium mixtures. It is very probable
that the stability-of the polymer Is due to the fact that the first product of
the polyrecoubination reaction, namely the dimer tetrap on-vlothagel is a
completely stable compound (Ref. 5). The structure of polydiphonyl methylene (I)
was also conf:rmed by IR-sp*otra. On the basis of their results, the authors
concluded the ft1lowingi tertiary butylperoxide decomposes in such a way that
I sole of peroxide develops only I mole of active radicals instead of 2. Bence
the maximun *f the molecular welghtt 2 mole* of peroxide consumption per I mole
of hydrocarbon. Half of the liberated radicals which developed originally, are
used for aid* reactions. From the above-sentioned compounds and others given
in table I the authors in the same way produced linear polymers with a high
molecular weight, soluble in benzene. If dureneq ditolylmethane, p,p'-di-iso-
propyl diphasyl, benzylacet*te or other compounds are introduced into the
reaction Instead of diphanylmothans, large amounts of indissoluble polymers
develop besides linear polymers. Their structure apparently is cross-link*d by
mothyl groups. Polyrecombination allows the production of linear polymers with
aromatic cycles not only in their aid*-, but also in their main chains. Finally
the authors state that polyrecombination will only produce linear polymers of a
Card 2/3

The ProduotLan of New Types of Linear Polymers by S/02Y60 132/02/32/067
Means of the Reaction of Polyr*combination BOII B002
high molecular weight, if tbo compounds used do not contain groups which may
act as branch poimts of the polymer chain. Thor* are 2 figures, 1 table, and
14 references, 7 of which are Soviet.
ASSOCIATIOWL Inatitut al omen toorgani chookikh soyedineniy kkademii nauk SSSR
(Ingl4jule of Momon1*1 Organto Compounds of the Academy of Sciences,
SUMUTTEDs Febrmary 3# 1960
Card 3/3

bibliogr.red.;
MMSKATA, R.N.; rRMXKMI, S.Ta., red.;_A~~~ T
OXIMIN, A.A., vedush*My red.; SILICHNIMOVA, V.V., telchn.red.
EBV~liovrsphla Index of works of scientific pereonnal of the
Ina4itute of High X61scular Weight Compounds of the Acadeor of
SciOnoes of the U.S.S.R., 1949~-1959] Bibliograficheskil ukasatell
rabol, asuchnykk actradalkov Institute vysokonolskaliarnykh soodinenil
AN MO, 194,9-1959 ". Sost.R.M.Tilenskala. Pod red. S.IA. Frenkells.
Leningrad, 1961. 103 p. (KMA 14-.2)
1. Akodsmiya awak SM. Institut vymokonolakalyarufth soyedinenly.
(Bibliogrephy-Xecrosolecular compounds)

27570
I 5-_,gs To 1$11 22,09 2405 03,"C "~'/005101 6
31 0"'=_IC1
AU"'HOILS: V. V., Sosin, S. Alekue-,reva, V. P.
Of rl--'W t~' Q 13 Of :ilEar
C JLL so.~edineniyj_ v. !, nc. 9, 1961,
133-:-1.34 0
TEXT: 'I"n efirst two authors o).iorc:! in, _,re,.ious ra-,crs ("of. 1: Dokl.
AN SSSR., 121. 299, 191~~b; Ref. 22: . . t~ - I that
et, - SOY 956 , 1959)
rhen treating joproxides (PO) of cumpo,.illAs such as 1-diisot ropyl benzene
( DIIjB) v 4iisopropyl f errocene , p-dich~' oro bunzene , et c. , iine&r polymers
are fornod, alldt part i cul arly in the ca.,le of Dli'_R, non-fusible and
insolutle polquiers with cross-linked txiner structure. Iclyrecombination
of iiph4nyl mothane phenyl acetic acid =ethyl ester, benzyl
etc.' -;af; studied ill the prvacnt work. *,.ti-n treatinI.- these
ct~npcurwltj with tort-butyl peroxide ratio af TBPO to inititil
conji,uaii ~~ 14) at 20COC, linear po!3-mara werv obtuinei. Diphenyl methane
(DPI:) 6,;Lve a. 'iiliear polymer, Un -,eilL~41SI! which
.11C~I
~.',:!nzene
)k :0. ::-Itculfir wei"ht
dissolvi-d Ir.
(meltinji point
Card 117

2757LI
S/1" ( l Ac 6
Synthonic of' ltew types ...
(1,:) of 1C.;DC10-'SIC~0,000, t:upendinj- on thin molur ratic.
c . 3 --, a. rc,~.t, -n- tal,.cI
The fc,
(d 3)3 CCC,C(Cll 3 ---+ 2 ( C113 ) 3CO' ( R' (c11 03 cv* (c:1 51-icc, + c1l3(w). ~1:0
radicals roact with the hydrocarbons:
R'- 1%1I 2 (Calish(Ill -Ifc (c.ll,):4Al
fc,14h - If V; if 0).
"he renultunt polydiphenyl tothylenc, (YD (1) dl-c~ icccmp~)tw to fr~,c
rad'calo in thit Precence off dipherayl pi c ~~:.j i,.i stable t,
oxidunts since the structure of t , t vi, T whi ch is
probably initially does not permit t!.e f :;tab], radicals.
Rearvan~:umentu :.,.ight take place, accLv-4ing
0
(n)
J
Card 2/7

27570
3/19 61/003/009/005/016
.7
Synthesis or new types B11 OX101
oh W 9 in visconity. In A, TPH is formed,(melting point, 209-2110C, i.e.,
higher that the reaction temperaturs),,and viscosity considerably
increases. In Do how
veri It, decreases sInce the lou,molecular polymers
melt already at 160-1 OOC. The reaction of TPS which in first accelerated
;
Is then retarded by the formation of high-molecular pulymere (melting
Point 20000). The viscoatty will be reduced toward the end of the reac-
tion by adding a DPX-?O mixture-, to DPMj the yield increasee. Peroxide
admixture of > 2. moles/mols of DFM graphically results in a steep ascent
of the mol.+cul&r iveight which asymptotically approaches the ordinate.
Assilming that,the chain grove by doubling (dimer, tetramers octamer), the
followizW holds: N 2 - 2/n, where N . number of free radicals/inoleal
R
A 0 polymerizatlon coefficient. I mole of free radicals is formed on
decomposition of TBPO. Uaximum V is thus obtained for a FO consumption of
2 moles/mole of hydrocarbon. 0.66 mole tort-butoxyl radicals result from
I mole PO (in tho form of tort-butyl alcohol). 1.32 mole of radicals
decomposes to giTe 1.32 mole acetone and 0.66 mole methane, as fvllows:
190-2000C-

1101
(CH
00* 1. (CH )2CO + CHj, and (B)
(A.) (CH (CH
)3C0' 3)2C0
)
3
3
3
3
+ CH _O-C-(CH3)3. According to Yu. A. Alekeandrova, Huan YU-1i, A. P.
Card 4/ 7
.
slim

NNW.
27570
S/190
./61/003/009/005/016
'
now type* BIIOIB101
Synthosl* of
change im viocoo kly. In At TPS Is formed.(molting point. 209-2110C, i.e.,
higher than tho reaction tompetaturs), and viscosity considerably
increases. In B, howevert it.d*oreases since the lov~molecular polymers
molt alroad.T at 100-1~00C. The readtion of TPL which is first accelerated,
is then retarded. by the forisation of high-molecular polymers (melting
point 20000). Tho viscosity will be rodubed toward the end of the reac-
tion by adding a DPM-PO mixturrito DPI11 the yield increaaea. Peroxide
admixture of >Z molee/molo of DP11 graphically results in a steep ascent
of the molecular veight which asymptotically approaches the ordinate.
Assuming that ib* chain gro by doubllng (dimer, tetramer, octam
r), the
:
N 2 - 2 P where N number of free radical /moleal
following bolds;
R
a - polyuerltation coefficient. I mole of free radicals is formed on
ditcompooltion of TBPO. Maximum U is- thus obtained for a PO consumption of
2 Dol
s/4ols of hydrocarbon. Me mole Ort-butoxyl radicals result from
:
I mol PO (in tbp form of ter%-butyl alcohol). 1.32 mole of radioals
docomposom to ViVe 1.32 mole acetone and 0.66 mole methane, as' follows:
190-2000C
(A) (CH5)500. '&I, (CH3)2CO + CHjs and (B) C (C11
(CH3)3 0' 3)2CO
+ CH 3' O_a_(OH3)3 According to Yu. A. Aloks&ndrova, Huan YU-1i, A. P.
Card 4/

27570
8/190/61/003/CC9,1005/Oi6
S.vnthesio of n*v types ... BIJO/B101
Pravednikov, Sj. S. Medvedov (I)okl. AN SSSR, 123, 1029, 1958), no methyl.
radicals are flormed in (B) which taken place at higher temperatures.
IsobutIleme oxide results on initiation of. the peroxide decomposition. The
authors separated the fraction (51-5300: isobutyl-methyl ether and
180tutTleme OCidu. In the same way, they obtained polymers which dissolvej-'
In benwane. When using ditolyl methane instead of DPRI a polymer
Inecluble in tionzene and p-cresol (melting point 180-24000 with cross-
linked structuiro is obtained in addition to linear polymers (melting
point . 150-161000, molecular weight - 2500). The elemental-organic
polymers obtained from dileopropyl ferrocene, ferrocene, and triphenyl-tr:V-~
X-isopropyl bor&zol (TPNI) by means of polyrecombination showed IR
absorption mmima at 820, 1000, and 1100 cm -1, and, accordingly, stru
cturo!
\qC11
ED
M 1000 7000 they are dark-red powders soluble in benzene (softening L
int -_3000C~- The electron paramaUnetic resonance signal (line width'
PO
Card 5/7

4
27570
5/190/61/003/0C9/005/016
Synthesis of mew types ... B11013101
.'A;
120 oat 2000 confirmed the existence of unpaired electrons (concentration
1021A polymer). Treationt of TPNI with TBPO yielded only a soluble,
low-nolecular polymer. Polyrecombinatton gives also polymers with
aromatic ringui In side and principal chains. A soluble copolymer was
obtainiod by triosting a mixture of DPhl (0.1 mole) and DIPB (0-1 mole) with
0.25 mole TWO; DIPD alone gave a nearly insoluble pol;rmer. 2,5-dichloro
p-xyleme gives a chlorinated analog of poly-p-xylene soluble in benzene.
C1 In ortho-position to the CH3 groups blocks them and prevents their
participation in the fomation of linear chains. Polyrecombination thus
results in carbon chain polymers with aromatic rings in the principal
chain, whose production is difficult. Can chromatography of DPM was made
on the X -2 (Kh-2) apparatus. There are 4 figures, I table, and 18 refer-
ences: 6 Sovist and 12 non-Soviet. The three most recent references to
Rnglisb-laneusj~e publications read as follows: Ref. 7. G. A. Russel,
J. Amer. Chem. Soc., 1-6, 1047P 1956; Ref- 9: J. H. Brook, Trans. Faraday
Soc., iu, 32T, 19571 Rot. 10: K. Id. Johnston, G. H. Williams, Chem. and
Chem. Ins. 1956, No. I 1@ 328.
ASSOCIATION; Inatitut elementoorganichtskikh acyedineniy Ali SSSR
Card 6/T I~Instituta of Elemental Organic Compounds AS USSR)

SOMN, S.L.1 XORSHAX, V.V.j ALUSEYEVA, V.P.
Polymer's and copoiYamrs, of derivatives of ferrocens obtained by
the p*Iy"oombIn&ti*u method. Dokl. AN SSSR 149 no.2%327-329
W 063. (KRA 160)
1. InstLtut elementoorganichoskikh soyedinen1y AN SSSR.
2. Chlea-korreeptedent AN SM (for Xorshak).
(Forrooene) (Polymerization)

III, I I
. 11N, T.. 1.. 1 V.V. i AUT ",-: 1~:A?A, V. I .
Poits~*,!-Atj of preparIng ~: gl-mlq~ular weight ~nmp unds
.0
fr-on (Iiphimilgermwia u,%dor vrailtionr -~f polyrecomlina--icr.
nj,uT~Aor. 'Iyoolcom,soed. 0 r1o. 518,,-'331 My ,t4,. (KIRA 17:6,
'. elertpntccn.gAn~ S3.511R.

ACCMSION"KRi 'VhCt32577-.-----.-- S/0290/64/006/004/07)i/070-!;
AUTHORSv Sosin, S. L.; Norshak, V. V.j Alekseyeva. V. P.
TIME: A atud.T of the possibility of synthesising high molecular compounds trom
diphonylsilsne undar conditions of the polyrecombination reaction
WUME: lryosolccmolek. scoredin., v. 6, no. 4, 1964, 745-750
TOPIC T41GS: oripanosilicon compound, diphanylailane, triphanylsilane, tetrapheWl-
silane, pharWlmilama polyrocombination, phoAylsilane haterochain polymer,
tatrapbonylailmob polymer, cLiphanylallane disproportionation, UR 3D spectroscope,
'Trub Taubar spectrometer
AMr'=T: The pol~jvacombination of diphenylailane was conducted in the presence
of tert-butyl peroocida in a special apparatus at 170 and 200C. The reaction
products uare troatod with benzene, and the soluble polymer was precipitated with
mot"nol. The obt-ainod compounds were fractionated, analyzed chemically, and
exa.minod by infriwed spectroscopy on a UR-10 apparatus &rA on a nuclear magnetic
resonance Trdb TIlubor spectrometer. The main polymer isolated by the authors

AGC=10's 1416 AIPLO325T7
is aucrilDod the Xormula
CIN
its 'o-=ation max li~ivo proco(XiCd (,J~11 Ll'.~' intermediate product totraphenyl-
ir
slla~a, -wlch ha!I betin i~olatod Ir'o'n Products torether with
n.A. hydrosilicon. Since itt, a 1:0.1 molar ratio of the issuing
diphc,-,~rliillano anil poroxid-) only L% of ddphonylsilaxie could be recoverod, it is
az;.,;U,-",d a d'.40~1.'Oporlvionation reaction t4kos placo in which some of the
produc~,:3 b,D,-.omo ~.-n,olved in the building of the polymer chain. T1,ds assumption
i3 sup.poi~.od by Vitb fact; that increased concentrations of the peroxide result in
a hirnor y-lald of tatraphonylsil=o. Heatirg of the obtained polydiphanylsilane,
of molocular weidit 1530 to 9000 in a quartz tube yielded a polymer with a'molecur.,",
iar wai[~at nf 810. Ilia bonzono -insoluble fraction of the diphorqlsilane poly-
rocorabin&tIon raamtion products yielded a po3,vmor of 190 500 molecular weight.
Orig. art. hass formulas and I chart.
',-C.ed 2 3

Acczs5lori M,: AFLO32577
lnotiLut ol(unentoorgaacheskilch coyed:Lneniy AN &SSR (Institute of
Qrr,&noolo-,r,.tntal QwVounds,AN SM)
3U-B'.ZTTz;-..) i OIJU63 DATE AC~3 1L%IaA4 =Ls 00
SUB CG-JZ-. CH NO Ra SOV 1 005 0-IfER a 009
Ca. d 3r)

UCESSIO~ MRs A14437M S/0190/6h/006/005/0827/0631
AUTARORSs Sovin, S. r..; Korshak, V. V.; Alekseyeva, V. F.
TITLEs A study oir the possibility of obtaining hieh molecular compounds from
diphenylgermanium under conditions of the polyrecombination reaction
SOURCE3 V7".okcnoleku1yprny%ye scLvedinsnlya, vo 6, no. 5j, 1964, 827-831
TOPIC TAM: diph-on:r1germanium polyrocombination, diphenylgermanium high molecular
compound, dipherWlgormanium disproportionstion reaction, diphonylgermanium diapro-I
porLionation product, tetraphenylgermaniwa, diphenylgermanium, germanium hydride
ABSTRAM The po:Lymcombination of dipherwlgormenium was conducted at 200C (in the
presence of tert.Wt I roxide) by a technique described by the authors in an
earlier publication Vyftok*aoleka. amrod. 3, 1332, 1961). The reaction product was
treated with bensom, and the soluble fraction vas precipitated with methanol. It
was found that tbo disproportionation of diphenylgennanium produced 50% of a po.13mw
Cam

ACCESSMN NA: AA037279
(with a maximum Molecular Weij~ht of 1840) and also tatraphenylearmanium, triphenyl-
germaniunj and gemnium hydrIde, the presence of which was confirmed by infrared
spectroscopy. Tito thers"I di6proportionation of diphanylgermanium also took place
without tort.butyl peroxide it 200C and at 1400. A copolymer of diphonylgermanium
with diphwVImU%nae in *qQix*Ur ratio was synthesized in the presence of tek.-
butyl percizids, y1m1ding an amorphous brown product with a t%olecAlar weight of 48M..
Orig. art4 hast. 4 formulas,
ASSOCIATICKs Innatut elementoorganichaskikh soyed1nenly AN SSSR (Institute of
orC&wgl4mnt&lCompomds, AN SSSR)
SUBMr= I 01juno DATE AOQs 09Jun64 MW OD
SUB OODRt W NO BW WV& 004 OTMI" 005
,card 2/2

SOSIN, S.L-1 KORSHAX, V.V.; A",EY-EVA., V.P.
Posed.biliV of syntheaAming m&crclaoleoular compounle from
diphwvlailane under conditions of the polyrecombination
reaction. Vysokow. soed. 6 no.4s745-750 Ap 164. (MM 17t6)
1. IntitItut elwwntoorgaLnicheakikh soyedinerdy AN SSSR.

VILEN.IKAYA, Utz& loarkovna; FRYI;KELl, S.Ya,, doktor fiz.-nit. 4 -
nailkp red. I .&LAn;. gVA,. '-'. 1., rer. I
.. red.; h
[HJjrh-m3le&ular ccir,poums; bibIlograrli!c index c. Soviet
ml rareign books, 193C~19631;1 7yz3okom--!CkUlAdrryc soedlne-
nlim; brIbIlografichaskil ukazatoll i Zaru-
b9zhnykh knie, 1930-1963. lAniiiWrad, 19(,~. 30L1 1:.
~vm.' 18:3c)
1. Aknda:-.iTa rAuk SS,51- Diblioteeka.

,AjL-Fs;,Il-r-WA, T. S.
Nervus -
S-urgic.-l 1.1jer.-Ty cif jerLpheral parallyse of t1le fmcial nerve (armstomosis of facial
&34 acc-,-,ssory nervim), Vop. neirokhirt 16p No. 3, 195'.
Vonthly Liptaf RiampLam Accemnions. Library -)r Con~~"-ss October 1")52 ll:r~LAHIFED.

CUzkc&l ASPOcts AZA surCiCALl tharaW of neurincza of the Ckkaserian
cavation. Top. nelmoichir. IS n0.5.-17-22 3-0 054. (MIRA 7:11)
1. lis lastituta usyrokbIrargil Iment W.31.3urdeuko Akadeall meditsin-
sbdft nso MR.
(Mmm' TRICUtILL,
caesarian ganglion, nsurll~moaa. surg.)
Cassorim ganglion, surg.)

ALIMUMA, V.S., Icatd.sed.naut (HOOkWO
,- ......
V44taloblastnes of the posterior cranial fossa in adults. Top.
notrokhIr. 2) *9.6t30-3) N-D 859. (KIRA 13:4)
1. Wanchno-iosledovatel'skir ordens, Trudovago Krasnogo Znaveni
luctitut neyrothirurgli luezi alcadealke, N.N. Burdento ANN SSSR.
(KERMU)SLAMM)
(SKM neoplasm)

A,=I=A,. V.S* kJodomedoun*
Topaigraphy of intracerebral t=mv of the parletal lobe. Probl.
s*vr.naIro]rhIr. 3a9g-IU 159. (mm 16 it)
(MAM-WCM)

AL=EfVA,. V.8., kandaied,=*
CU14ca.1 aspects and aurj;',~:al trzem'rimit of nodular bones of
swoomas of the earebellm. Probl.sow.neirokbir. 4WO-234
~62, (MIRA 1612)
OMMUMP.-TUMOM)

50) SOV/79-29-9-41/76
A L'Ua S s Lutokiyj A. Ye., Ileksoyeva, V. T.
TITLIt Intramolecular Hydrogen Bond and Absorption Spectra in the
Ultraviolet. VI. Absorption Spectra of Nitro-aniline
PUNDICLLs Zhurnal Dbehahey khisail, 1939, Vol 2?, Nr 9,
pp 2992 - 2?98 (USSR)
IB$"LUCTs The absorption spectra of o-, m- and p- nitro-anilines
were frequently inveatigated by spectrum analysis (Refs 1-9).
The characteristic features of their spectra are explairied
by the formation of quinoid stractures (Ref 1), by the vary-
ing stability of thq intramolecular bonds of the isomers;
rwithout explaining thtir nature) (Ref 2), and by the differ-
t
ence in their energy levels between which electron tranvitions
tako place (Refs 7,800). On the basis of the phjsical e.nd
chemical properties of thLse compounds (Refs 11-14) the intra-
molecular hydrogen bond is assumed to be only present iu the
ortho-isomer.
Card 1/3

W
rrit.i-amol+(jultir Hydrogen Bond and Absorption Spectra SOV179-29-9-411/76
tn Ine '01truviolet. VI. Absorption Spectra of Nitro-aniline
0 %N~ 0
Th4- relation between the individual absor-otion bands and
certain kinds of electron tranaition is bound to be reflected
by the kind of its variation when another solvent is used.
Pot, thig reason the aothors determined the spectra of nitro-
benzena, aniline, and o-, m-, p-nitro-aniline in six differ-
ent solTents which had hitherto not been used for such in-
vestigation3, i.e. benzene, chloroform, diethyl ether, n-bu-
tdnol and sulphuria anid (981p and Figures 1-6 show
the rovilts of invcjst.`,~ation. Thiy rcvca: that the character-
CII.rd 2,13 istics of the nitro-aniline spectra are similar to those
observed It, "all di3u!;stitutcI' benzenes with actIve groups,

intram-.1411:ular Hydrogen Bond and At-sorptior. SPeCtrs SOV179-29-9-4
in I!ie Ultraviolet. VI. Ab~)orntton S:Iectla cf Z-4tro-aniline
obocryed in all disabatituted with active grCa..'s,
I.e. with a mzcleophilic an! group. The lanz-
i
wave band of nitro-ai-~ il ine3 -:i ~-.r 1: ---~ V-band of electron
transitions in which the electr_).,-.c cf both functional grou;s
take part. In o -nitro -ari I ire the in-razolecuiar hydrorer.
bond is cham;terited by a distir.cl shift and broadeninZ ~f
the band (A) toward the long-rave r3nEr-. The table shovs
data characteristic o:t tle abn,:r7tion spectra of n4 tro-ard-
lines. Thert are 6 f.Zares, I taile, and 2_6 refcrences, 8
of which are Soviet.
k.SZ.,.1CI17l0:It Lhar kovalci;r kolitCLI- -' C!. e S 11 j.-,st-tat (KharIkov PoLrtech-
nic lnstit-at~)
IS U ZY, I T T 1:1) tJ*JIY 27, 1958
C it r 1. 31/ 1

~ " 1) 1
It, SOV/73-29-9-42"76
A Ye., Llekaeyova, V. T.
"ITLLI Abnorption Spectra of Dinubstitated Benzenes With Functional
Groups Acting in the Same WRY. I. Nitro-acetaphenone
FLR:OLI-~kLt ":!iurnul obahchoy khimii, 1959, Vol 29, I;r 9,
FP 2998 - 30o5 (USSR)
A -IZACT i 7o clurify the nature of the clectron transitions which
correspond to the various ultraviolet absorption bands of
%he aromatic compounds, it is necessary to investigate the
characteristics of absorption in the case of diBubstituted
benzenes containing functional groups acting in the same way.
The spectra of the compounds of this kind (nitro-acetophenone,
nitro-benzeldehyde, dinitro-benzene, etc) have been investi-
gated several times (Refa 1-8), as a rule, however, only in
hexane or ethanol without consideration of all isomers. Know-
ledge of the character of the variation in the absorption4bands
in polar# hydroxyl-containing, and acid solvents is necessary
Pefa 9-11) for a determination of the nature of the electron
trans"tions. The spectra of the compounds of this kind were
Card 1/3 :Lnvea;ir,.Z.d in the following seven solution's: in apolar ones

Absorplion Spectra of Disubstitated Benzenes With S 07/79-29 -9-42/76-
F,.Ln,::tIonv1 Gro',apa Acting in the Sam$ Way. 1. Nltro-acetophenone
(~wxave, b(inzene, dioxane), in a polar solution (ether), a
hpiroxyl-containing one Cn-butancl) as w(,Il as in 98 and 9.0
isulphuric acid. The reaults of mLasurement of the spectra of
nitro-benzene and its o-, m-, and. p-acetyi derivatives in the
arorementioned solv--nts are givt-n. The absorption curves of
tittro-acetophenonas are similar with respect to the number,
and pcisition of the absorption bands as wcll as to the varia-
tion caused by the natare of the solvent; this similarity re-
J'-vrs also to the absorption curves cf the morusubstituted
ouwpou,nds (mainly nitro -benzene) . The --haracteristic features
of the, spectra of the kinda of compounds under invcatigstlon are
doc, ta the hindered transition of the cliarce in molecule exci-
L!iticr. under the participhtion of the electrons of both substi-
t,lents. The pro-cence of a nte-ri~,- affect af the groups is only
,::(;nfImed by The I-ards corresponding to
Oiv P ---*It trnrisi+ions do not undergo a hypsochromic shift
Lti hydrogon-cozitnini;.6 avivents and anids in groups with
t- and some p-ulectron pairs. Th~-rc are 11 figures, 1 table,
Card and 21 referencea, 4 of which are,- Soviet.

Abuorption Spikatra of Diu ubst ituted Denzenes With SOV179-29-9-42/7.6
Functlo-nal Groups Acting ir the Same Way. 1. Nit rc-acet o;henone
AS$CCIA7lO-': J,", r1kovskly politekhr.icha3kly institut (KharIkov Polytechnic
tnstitite)
S"JBILIMiDs .7uly 27, 1958
Card 31r3

LLTSKIY. A.Te.; 4~4R VA. I.T.
Aboorption spectra of disubstituted benzene derivatives having
fumotional groups of the sanA directing influence. Part 3:
M brobemoic acids and athy-Initrobensoates. Zhur.obAchim. 30
no.S-.2737-2742 Ag '60. (MIRA 13-8)
(Beamoic acid-Spectra)

IMUT, A.U.; AMMMA, V.T.; 011DRATUX0, D.P.
Dipole mmmU of disubotituted benzenes baying electron-
Acceptor functional grooph Zhur.finskbim. 35 no.8:17D6-
1709 Air 061. (MIRA 14:8)
1. Mwrtkcffakiy politakhnicheakiy institut imani V.I.
Uni".
(Demsene-Dipole moments)

PUM I BOOK EMAOrMATION SOV/4769
Ostrouebko, Tu. I., P. 1. ftabikhin, V4.XL.ALA#seyev&, T. F. Itaboyshchikova,
0. A. Kov&, S. A. Shielkova, R. N. Alekseyeva, -aid M. A. Makovetskaya
Litty, yego XbL=:Lys I tekhaologLya (Lithium, its Chemistry, and Technology)
Mucow, At4u1zdLt, 19W. 3.98 p. Errata slip inserted, 5,000 copies
printed.
Ed.-. Ye. 1. Panasenkova; Tech. Ed., Ye. 1. Ma&ell.
PURPOSEt lhistook In Intended for scientiric workers, metallurgical engineers,
and. obadato working in Un abomistry and technology of rare and sparsely dIs-
tr1bated elements. Engineers and mechanics In charge of lithium production,
and. stu&mts In schools of higber education and in tekhnikms may rind the
book useful.
CMRAGE: The book deals with the Seochemlstry and mineralogy of lithium, the
cheakistry of lithium and Its compounds, aniLlytical chemistry of lithium,
a of lithium ores, methods of processing lithium ores, and the aetal-
CsAft- . ..6

Lithlun, Its Mmmistry, and Technology (Cadt.)
SOV/JT69
largy or lithium. It is based on SovIet and other technical literature
published from .1918 through 1958. No personalities am mentioned.
References accompany each chapter.
TANA tt CONMUM:
Ch. 1. The Gahkahemistry and Mineralogy or Lithium
Geocbemical ataristlas of lithium
at*ariatIcs of 11
lithit" in natur
Occur 2no, lithitu in nature
Speci . f t of the geochemistry of lithlun
=~ 0" 2. geocha
its
Types of 311%blum
MineraloSy of 11thl
Silicates
Silicates vith unbro chairs of tetrahedra
Silicates vith unbrolk. rs of tetrahedra
SkelmUtL allIcates
Carwaft-
7
7
8
9
12
12
12
20
23

-OSTROOEM, YM&rj ALMMMA, V.V.
GOOU*rjma W"wo an a potentlAl stwurce of Uthi=6 At0asuerg. 10
40o4419-420 AV 161, (Lithim) . (MBA 14 14)

ALUCMUVJL, T.'rowebm
'JIM
QLSO of cfrrvicsl pregnancy. Aftsh. I gin. 35 no-3:114-115
W-jo '59. (KIRA 12:8)
1. In rodillnogo dam No.22 (slavVy vrach L.T.Ostrovityanova)
Garodskoy klWahookor bolluitay No.2.
(PEW&MY, ACTWIC
cervical (Rua))

NMCIIAYCMZO Xilcolay Ponteleywylob; NUMATCHN. Tovgen4 Nikoloyerich;
PURM. S.. kand.tokbu.nouk, retseuxent; ALIL59MA, To.. red.;
TOMMA. Z., tokhn.red.
CUltrasonics In the national ooonmy) Ulltroavuk v narodnom
khooloistys. lxhovski, Udomrtakoe knixhnoo lmd-vo. 1959. 54 p.
(MIRA 13t12)
(Ultreawde ways s-Indum trial applications)

ALD:5!rf~:;:, Tt. A.
XNPQMW. M. I
Motor function of the wall Intention In Addison-Blermar's anemias
Tersip.arkh. 29 no-3:85-89 Nr 157. (KLPA 10:8)
1. 12 fbkulltetsicoy terspertichaskay kliniki (dir. - deyetvitellayy
cholm, ANN SSHR parf. V.S.11nogradov) I Mosiroveirtgo ordena lanina
seditsinskago imatituts isont I.K.Sechenova
(AMUNIA, PXRZCIOUS. pk7siology.
intestIne, swell, motor funct. (Run))
[INZW10. 8VALIss invarious diseases
anamis, pernicious. motor funct. N,))

, r-1. fl~.
5773. 1-im-ir I fj~ I f vt i, I m-v, -,is rs +nw,o ;-rtntt v v -fl- n~ t~ ' . ' '. - , f
I I -, '_.. 14n. S ill
21" (1:-" trnn.-r,. ll.!',~~14. *;r,--m-,jj-. F-
v--jrt,n_t~',`rcj. i--t.
*;PTT.- telhn. vr~. 116). 4o") -k-. ". ts.-'t. T'.,- I y C.-
( 54-15002',") 45.9.0W- ~,67.67.
!-'o -Kni?!ir,.qva. L-troj)5~, Voi_ !, 105~-

AnXMMA.#,. U.A. p ksPd.m*).!mkokbo1MstT*ucwkb nauk; AIMIRL ISM19 S.A.
241b-oeld oo)Amtod vwIstimp *f mint for production. Kaslo-Wdro
peabs. 26 no*5131P-36 * 160o (KML l3t22)
2. lrdomwfuww~, usuebuo-la"afttells3dy imtitut mulicbsWkb I
eftl"Wullchqft'~ kviltur.
(10rumodar Territory-4%pperadnt-oil)

R1.1'MIXG, III id &a! I 71~-liyovktovicb, A&nomik it 41.
I At ry I, 1107.1ch; C!Ecl'-.'~;T, Yu.3. , J:rcf., r,
-W, -c,]
USSP-%~, A.!-. karld "kkm. rin
dclktor tokht~. riliuk, red. ; h4..
red.; Ye.h., reed.
...... ..........

TXALU, lvtu,; MikhaTlovich; I'M*RGV, V.A., ret4lenZent;
SHTIMNWAIDM, X.B., inzh., muchn. red.; AUIL__71___Iv_I
~2.4. . red.
[ A.Paembly -line production of electrical inst-Inimentsl
torlmoe proizvodatwo elektricbeskikh ~riborov. Mosk-ot,
Eneeglia, 1965. 30 p. 18:7)
2. '.avud "Vibrator*, Leningrad (for ShteymOmayderi.

DMiROVSWIA, K.S., dektor Made sIdIh nank; A.LEKSEYEVA, To.A., inzh.
Incr*saizg the wear resistance of metals by chemical *at
tnistwent. Trudy NIIKHDNUII no.271142-3A9 159. (MI*RA .14: S)
(Came hardenimg)

5(2.4)
AU711ORS: Dombrovakaya, N. S., SO-7/2C-127-5-24/58
TITLEi A Mutual 7~Component System of 16 Salts of Li, Ila, Rb, Ti 11 Br,
C3., Ito 3' 304 'n Melts
PERIODIC"jUl t DoIclady Akademii nauk SSSi, 1M, Vol 127, Rr 5, pp 1019-1022
Ossn)
A35"'BACT. lProm the practical point of view the investi-ation of multi.
oomponent systems In of high importance for ~Ije investigation of
iuLtural and technological processes. A con1lete investigation of
auo.,b systems is very complicated. llet%ods of a si=rler solution
of these problems were shown already in the thirties by N. S.
Euxnakov and his collaborators (2efs 1-4). The composition of
thm mentioned systems is repreaented -or-actrically by n-diman-
vional polytopes. The ayaton, mentioned in the title which wav
investigated by the authors contains the following systoms of'
component3i
16 syztemsaf 1-components of tho type AX
46 binary systems of the ty;~e XX - DX
3.2 ternary systems of the type All X, Yj Z
36 ternary mutual systems ot the type A, 3)11 X, Y
Card 1/~. 8 quaternary systems cf th:- t~-po All.'Ir Y, Z,

A Mutual 7-Co33 onent Systen of 16 Salts of SOY/2C-l 27-5-24/58
L1, Nn, Rb, Till Br, C1, so 3'S 04 In Melts
411 quatnrnary mutual systems of thc t;
I ;c A, B 11 x, Y, Z
It! quintary mutual systems of 0 i~alts A9 BlIX, Y, Z, T
16 quintary nut-jal systems of 9 saitc A, B, CIIX, Y, Z
,9 ht~xadic mutual systerns cf 12 salts At Bt C 11 X 1 Y, Z, 7
1) n t e r m i n a t i c n of the t I n E u I a r s t a r
Such an (equilibrium) star ir delermizied by th-~ stable diagonals
or the ternary mutual vyctems, %- the stable -11nSonal triangles
or the quaternary tautua3 systema, by the stable diagonal
t4itra.hedra of the quintary mutual eystens etc. (nefs 2-4). it is
practical to use the table of indi,:tca of the pilyte.,pe peaks which
,rqtr,p used for the geometrical representation of the compositions
Of multi-conponent systemB. the pe--k indices of multi-comyonent
syntoms are determined by the number of stable diagonals liarsing
through the polytope peak connerned. Talle 1 shows the peak
indices of the mutual systems from 6. 0, 9, ane 12 salts.
The Mu tual a y 8 t e m (as nontioneJ in the title) is a
0-dirienvionitl polytope (Ref 4). 2able 2 shows "he peak indicea
Card 2/5 fi:ir this polytope. The Eingular star :;ontqins the most ctabl.-

A Mutunl 7-Coni-Ditent System of 16 Salts of SOV/20-127-5-24//,re
Ll Na, 11b, Ti 11 Mr, Cl, rOVso4in Lelto
"bane" tetrahedron 9-5-5-9 L12SO 4_VaC1 - RbNO 3 -TlBr
(first montioned by V. P. Radishchev). It is placed in the center
of a cube and 6 pentatopes have it in common in the centers of
tho cube-facets; 12 base pentatopes are placed in the center of
Sun.dratio cycleol 30 hexatopes are in the middle of the edges;
20 hoptatopen are at the peaks of the equares and of the 2
prolongations. Figure 1 snows tho, oir4rilar star of the system
mentioned in the title. It I= a double sy=etrX with a center
of syt=etry. The menticned sycton L-ay bc attributed to the class
of the ravernible-autual systons. There are I figure, 2 tables,
aii.,! 0 Soviet referances.
PRESMiTIMs AP341 4, 1959, by 1. 1. nerrqayet, Academician
SLZLITTIM M%rch 30, 1959
Card 3/1'

-..r Ulu -,!;L r! ':2t
mr
I, cn'l i!'.j' Ulf) rrv I ce LIfe ~f --Ch I k-~~ R,
:1,1!0.~) cojer jx~-.t.rKl. ("erIcr: its: L.
~tit t
ELI 1 t~wj.. I B v: u t:
ry
f i ya k I f. C h n a
~11 co t' cvoit!~!.n~ t.: rr r ren t i t :-L: c' c
in Kiyev n !.c:;Avr 1,.,f'7 I"
tLe ~~arv.Lcc- 'Ife -Ac ----,,Iference
V) ~-d 1:'~ , I Ir 1t I, t u t v tr, 1111: d (1-nFtitute of
t-ructurti- thL- 1,cadet-L.- 1) m . 1:y the
'j hn -in.' cli,~' i-,) !icl-t!ctva ;ashinostnitelf
1('V Rel't-InL I i,in c To c hn ~' c n.1 So c i o ty
the