SCIENTIFIC ABSTRACT LEBEDEVA, N.V. - LEBEDEVA, R.N.
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CIA-RDP86-00513R000929110008-1
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S
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100
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Publication Date:
December 31, 1967
Content Type:
SCIENTIFIC ABSTRACT
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ACC NR,AP60358' 8 M, 4 CODE: UR/0413,66/oOO/020/003 003
IINVENTOR: Mellnilcov, N. N.; Grapov,, A. F.; Lebedeva, N, V.; Daragan
11. K.
iORG: none
i
'TITLE: Preparation of N-alkoxycarbl:)nylallcylamidoallcylth:lophosphonic
acid chlorides. Class 12, No. 187015 [announced by All-Union Scientific
lResearch Institute of Chemicals for Plant Protection (Vsesoyuznyy
~nauchno-issledovatellskiy institut khimicheskilch oredstv zashchity
irasteniy)]
SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znakI, no. 20,
1966., 36
TOPIC TAGS: fungicide,,
ABSTRACT: To o'btain N-alkoxycarbony,*Lalkylamidoalkylthiop'hosphonic
acid chlorides, intermediates in the preparation of fungi-~
cides, alkylthiophosphoni,r acid dichlorides are treated
with eaters of a- and 6-aminoacids in the presence of
tertiary amines, as the acceptors of HC1.
DIA-50; CBE No. 1LO
SUB CODE: 07/ SUBM DATE: 3lDec6,- (PS]
C,,d I A UDC:1547.233.2112211181-31:21113-07
LFIBEDEVA, N.V., kandidBt meditainskikh nauk
- I '* -
'ff ~~, t
=
sin'g ants in apoplexy. Mad.sestra 16 no.5:10--13 My 157.
OCRA 10:7).,
1. Is Inotituta nevrologii Akademii ma4itsinskikh nauk SSSR,
~ Hoe k-va.
(NURSES AND NURSING) (APOPLEXY)
GEELKNOV, L.G.; SHUTOVA, T.Aq KDEVA, N.V.
Clinical characteristics and theoret-l-c-87"basis for -the restoration
of functions following disorders of cerebral circubationLid-ith.,
summary in French]. Zhur.ni)vr.i osikh 57 no.2:161-1tyl '57.
(KLRA 10:6)
1. Institut nevrologii (dix. - prof. N.V.Konovalov) Akademit
madit8ins,kikh nauk 333R, Maskva.
(CFAMRAL HEMORRHAGA. ther.
posthemorrh. reatoration of tissue & of funct.)
ALEKSMVA, A.A.; LEBMEVA, N.V.; DUBNYAKOVA, H.M.
Clinical aepects of Venezuelan equine encephalomyelitis. Zhur. neyr.
i psikh 59 no-3:313-320 '59. (MIIRL 12:4)
1. Klinika virusnykh zaboleivaniy (zav. - prof. N.V. Sergeyev) Instituta
virusologii AMN SSSR i In.9titut nevrologii (dir. - prof. N.Y. Konovalov)
AHN SSSR, Moakws..
(EIIOBPMLOMULITIS, EquiNE,
Venezuelen (Rus))
BERGINERf V.M.; KUKUSHKINA, V.P.; LEBEDEVAy N.V.
Some data on the influence -6f-iiitravenbus use of e-uphyllin cyn
cerebral blood circulaticn, arterial pressure, arul respiration
following acute insult and under experimental cohditions. Trudy
Gos. nauch.-issl. psikhonevr. inst. no.96:303-310 '59.
(MIRA 14:1)
1. Inatitut nevrologii At-IN SSSR, Moskva.
(AMINOPHYLLINE) (BRAIN-DISEAS10)
(BLOOD PRESSURE) (RESPIRATION)
CHLENOV, L. G. (deceased]; LEBEDEVA, N. V,
Diagnosis and treatment of cerebral insults. Nauch. trud7 inst.
nevr. AMN SSSR no.1:44-61 160. (MIR: 1-5:7)
1. Institut nevrologii AW SSSR.
(GEREBROVASCULAR DISEASE)
KOLTOVER, A. N.; LEBEDEVA, N. V._
Acutely developing foci of gray softening in the brain. Nauch.
trudy Inst. nevr. ANT SSSR no.1:474-485 160.
(MIRA 15.7)
1. Institut nevrologii ANN SSSR.
(BRAIN-SOFMUNG) (APOPLEXY)
(CMEBRAL ARTERIa3CLERCSIS)
LEEFJWA?-y-To .,-
Clinical aspects and differential cliagrosis of lateral and
medial hemorrhages. Nauch. inform. Otd. nauch. med. inform.
AMN SSSR no.1:61-62 t61 (MIRA 16:11)
1. Institut nevrologii (direktor - deystviteltnyy chlen AMN
SSSF- prof. N.V.Konovalo7) 9IN SSSR, lbskva.
LOOLTA, N.V.
Determination of germanium in process solutions. Zav. lab. 30
noolltl331 164 (MIRA 189.1)
1. !notitut obahchey i n-sorganicheskoy khimii AN UkrSSIR.
ACC NR: A116033181 SOURCE CODE: UR/0079/66/036/010/1841/1843
AUTHOR; HeVnikov, N. N.; Grapov, A. F.; Labedeva, N. V.
ORG: All-Union Scientific Research Institute of Chemicals for Plant
Protection (Vaeaoyuznyy nauchno-iseledovatel'skiy in&titut khimiche-
skikh aredstv zaahchity raoteniy)
TITLE: Organic insecticides. XCIX. 0-arylmethyl- and chloromethyl-
thiophosphonic acid chlorides
SOURCE: Zhurnal obshchey khimii, v. 36. no. 10, 1966, 1841-1843
TOPIC TAGS; insecticide,-&e-4 chloride,
phos phonic acid
v-~~~~~~acid chloride /fv'~ 9-
ABSTRACT: At 5-15*C in absolute ether in the presence of triethyl-
amine, phenols react with equimolar amounts of dichlorides of methyl-
and chloromethylthiophosphonic. acids to form the corresponding aryl-
methyl- and chloromethylphosphonic acid chlorides:
'11PSC1, + ArOll + (C211&)3N
1AP(S) (0Ar)C1 + (C21f,)3N - 11CI
R =CIT. CICII'.
I ..
In the case of the formation of 2,4,5-trichlorophenylmethylthiophos-
phonic acid chloride, the reaction is conducted at -5 to 5 C to avoid
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he forma tion of bio(O-2p4, 5-ti:ichlorophenyl)methylthiophosphonate.
.
The acid chlo rides, whose composition and constants are given in the
table, are use d as starting mat:erials in the preparation of insecticides!
Orig. art. has t table. JW.A. 50]
'SUB CODE:4,07/ SUBM DATEt 065',ep6 5/ ORIG REF: 001/ OTH REF: 002
-Card 2 / 2
LEBEDEVA, N. V.
Construction of a Model of Convection and Calculation of the Quantity of
Showers
Tr. Tsentr. in-ta propmorov, No 31, 10,54, pp 3-35
The principal condition for the occurrence of thermal convection under
favorable circumstances is the heating of the ground layers of the air by
the surface of the earth through -turbulent heat exchange, in such a way
that up to the condensation level (up to an altitude of 1-2 km) dry-
adiabatic gradients of temperatur3 arise and super-adiabatic ones in the
lower 100-150 meters. In the layers below the condensation level the
temperature gradient must equal or be greater than the moist-adiabatic.
RZhGeol, No 3, 1955)
SO: Sum. no. 639, 2 Sep 55
IXBEDEVA,Nadez)sdFL Vladimirovna, kandidat fiziko-matematicheskikh nauk;
1' 17 redaktor; ISLYNTITXVA, F.G., telrhaicheskiy
redaktor.
[Hiw clouds and precipitation are formed] Kak obrazuiutsia oblaks,
i osadki. Moskva, Izd-vo "Znanie," 1955. 23 p.(Voesoiuznoe ob-
shchestvo po rasproutrane.aiiu politicheakikli i nauchr*rkh znanii.
Ser.3, no.17. (MLRA 8:9)
(Clouds) (Procipitation)
SOV/124 57-8-0146
Translat~on from: ReferaEivnyy zhu::-ral, Mekhanika, 195-r; Nr 8, r, 81 (USSR)
AUTHOR- Lebedeva, N. V,
TITLE: Vertical Motions Along a Front (Vertikallnyye d;,-izheniya na
fronte)
PERIODICAL: Tr. Tsentr, in-ta prognozov, 1956, Nr 45 (721 pp 74- 87
ABSTRACT: The author provides a practical calculation method for the
vertical motions due to friction in the frontal region, issu;-v from
the results of a paper by N. P. Dogadkina and A, F., Dyubvu~
(RZhMekh, 1957, Nr 8, abstract 9145), She composes aux'i;.Ary
tables wherewith to perform the calculatior of the vertical
along a front. The paper also comprises a detailed analys-'s of the
formulas of Dogadkina and Dyubyuk, In the conclus-Lon she adduces
a method for the calculation of the vertical motions, also for the
quantity of moisture condensed as a result of the rising motion. due
to frontal friction and nonstationary nature, A comparison of the
computed and the actual precipitation shows that the calculation
yields values one-half to one-third those actually observed. The
Card 1/1 author explains this fact by the disregard of convection effects.
V. P. Sadoko~-
V A ) /V. V
AUTHORS: Lebedeva, N. V.; Mishutin, D. A.; Pikush, N. V.
tTITLE: The Disastrous Cloudburst in Nikolayev (Katastroficheskiy liven' v
Nikolayeve)
'PERIODICAL: Meteorologiya i Gidrolog-iya, 1957, Nr 1, PP 37-41 (U.S.S.R.)
ABSTRACT: The force and effects of a terrific cloudburst (with lightning and hail)
which occurred on June ~30, 1955, in Nikolayev and its surroundings during
which time from 165.0 to 195.0 MM of water were deposited, are described.
Table 1 shows the amounts of precipitation deposited in various points of
the regLon affected. The dynamics of t1B storm according to pluviograph
recordings are analyzed,. Many homes were flooded, many damaged, and sane
canpletely destroyed. The asphalt sidewalks on many streets were demolish-
ed, stone bridges were washed away and trolley car lines damaged. The
water depth in some places reached up to 1 - 1.5 meters, the depositions
in some streets were 0.!5 - 0.7 m. Railroad causeways were washed out in
many places and the crops suffered immensely. Large numbers of wild life
(rabbits, birds) were killed. It was the first case in 150 years of
meteorological observations that the Nikolayev region has seen such a
cataclysm. Chart in Fig. 1 shows the distribution of precipitation in
the Nikolayev region on 6/30/1955. Fig. 2 shows the wvather chart at
2100 hrs.on that memorable day.
The condition of the atmosphere over Nikolayev at 1700 hours on 6/30/1955
is explained in Fig. 3:, and the air temperature changes in Fig. 4. The
probable causes of the cloudburst are explained on scientific bases.
3(7)
PHASE I BOOK EXPLOITATION
Tsentrallnyy institut prognozov
SOV/2114
Voprosy sinopticheskoy i dinamicheskoy meteorologii (Problems of Sy-
noptic and Dynamic Meteorology) Moscow, Gidrometeoizdat (Otd-niye),
1958. 110 p. (series: Its: Trtidy, VYP. 77). 1,100 copies
printed.
Sponsoring Agency: USSR. Glavnoye upravleniye gidrometeorologiche-
skoy sluzhby.
Ed. (Title page): A. I. Burtsev; Ed. (Inside book): . V. I. Tarkhunova;
Tech. Ed.i T.Ye. Zemt,;ova.
PURPOSE: This issue of the Institute's Transactions is intended for
synoptic and dynamic meteorologists.
COVERAGE: This collection of articles deals with various aspects of
atmospheric circulation. Individual papers discuss convection in
warm fronts, visibility during snowstorms, the relationship be-
Card 1/3
Problems of Synoptic and Dynamic Meteorology SOV/2114
tween fronts and jet streams, questions of pressure change, and
vertical motions in the atmosphere. References accompany each
article.
TABLE OF CONTENTS:
Uspenakiy, B.D. Conversion of the Vortex Velocity Equation Into a
Form That Would Facilitate, the Analyses of Changes Occuring in the
Fields of Absolute Topography 3
Pogosyan, Kh.P., and M.V, Shabellnikova. Jet Streams and Fronts 8
Bachurina, A.A. Analysis of Horizontal Visibility Near the Earth's
Surface During a Snowstorm 15
Lebedeva-, N.Y. Forced Convection on a Warm Front 42
-Le ~edev~aNV. Thermal Convection 64
Burtsev, A.I. A Method for Computing Vertical Air Velocity by
Taking Into Account-the Variations of the Vertical Temperature
Card 2/3
. Problems of Synoptic and Dyiiamic Meteorology SOV/2114
Gradient With Altitude 82
Turketti' Z.L., and V.I. Zhilltsova. Results Obtained From Testing
the Computation Method for Precipitations During the C6ld Half of
the Year in the Operations of the Central Institute of ForecastinglO3
AVAILABLE: Library of Congress
MM/bg
Card 3/3 8-13-59
HAKKAVEYEV, N.I., prof.; MIEDWA, N.V.; ZAITOV, I.R.; -LEBEDEVA, N.V,,-
YMVEDEV, V.S.; LAZARLITA, L.V., tekhn. red.
(Experimental geomorphology] EksperimentalInaia geomorfologiia.
By ITI.I.Flakkaveev i dr. Moskva, Izd-vo Mosk. univ., 1961. 193 P.
(MIRA 15:1)
(Geological research)
SKOHOPANOV, S.G., red.; DADYKIII, V.P.) doktor biol. nauk., red.;
LEBEDEVA V.V., kand. bil. nauk, red.; ',L4YEVSKAYA, V.S.y red.;
red.; SHO]MEISNA, A.V., red.; MEYVER, I.K.,
tekhn. red.
(Improvement of farm and forest lands in northwestern U.S.S.R.]
Velioratsiia sell skokhoziaistvennykh i lesrVkh ugodii Severo-
Zapada SSSR; material:,T konferentsii. Petrozavodsk, Gos. izd-vo
Kareltskoi ASSR, 1962. 253 p. (MIRA 15:6)
1. Nauchno-tekhnicheakaya konferentsiya po voprosam osusheniya i
osvoyeniya bolot i zabolocherzqkh zemell Karelii, Petrozavodsk.
1961. 2. Cblan-korrespondent Akademii nauk Belorusskoy SSF, X' mini-
aterstvo-oellskogo khozyaystva Belorusskoy SSR (for Skoropanov).
(Russit, Northwestorn-Soils)
LEBEDEVA, N.V.
Advantages of ther aerial wthod- of -studying bogs. Uch. zap. Petrozav. goo.
un. 127no;2t24-33 064. (MIRA 18:7)
ACC NRiAP6031057 A SOURCE rv'ODE:UR/0394/bb/004/009/005-1/00
A'WHOR: Balcumenko, L. A.; 14e'D Razvodovskaya, L. V';
Grapgv;,A.' F.; Mellnikov,
ORG: All-Union Scientific Research Institute of Chemicals for Plant
Protection (Vsesoyuznyy nauchno-issledovatel'skiy institut khimiches
~
Isredstv zashdhity rasteniy)
TITLE: Synthesis and herbicidal activity of amido esters and diamides
of methyl- and chloromethylphosphonic acids
SOURCE: Khimiya v sel'skom khozyaystve, v. 4, no. 9. 1966, 51-54
TOPIC TAGS: phosphonic acid,
-V~amide ) '7-0X'W0j_6C(1
ABSTRACT: Herbicidal activity of the previously obtained amido esters
and diamides of mathyl- and chloromethylphosphouic acids
was studied under laboratory conditions. The results ira
given In Tables l.and 2. Experiments with white mice
shovQd that asido esters of methylphosphouic acid are
highly toxic for na-anals, as showumin Table 3.
Card 1/5 uDc:632.954+542-91
_NReAP6031057
Table 10 Pz~oyerties. iknd'heirbicidal 'activity of amido eaters of methyl-
I-and- chloromethylphosphonic acids-
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.Table 2. Properties and ~'Mrbicidal activiiy of diamides of'methyl~-
Lphosphouic. acid.
HjC-- P - NHAr
NR.
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3.
4
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6
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8
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CH,Cl..u CH, 124-125 > 150 150 >150 '135 .120 37,5 >I 50 >160 >15o IoS
CoH,CI-n Clia 158-160 > 150 150 > 150 60 97.5 97.5 >150 > 150. 135 T
&20
CHCHa-A CH, ~ 86--N - -
. - 1
QH.CH&-n CHa 139--141 - - - -
QHS C.H. 78-79 > i5o m 75 75 > 150 >150 > 150 >150 > 150 .10
CGH,CI-o C3H6 .64-85 150~ 37,5 >150. 75 >150 >150 135 '135 120 >150
CH,CI-A CA 106 6-106 51 >M0
' 75 >t5O* 37.6 >150 >150 > 150 > 150 1>150 >JSO .
C4H.C1-A Wil 1;4-,114:5! 50
> 1 37.5 > 150 30 >150. > 150 J35 120 1
.>150 37.5
CH,CH,-O C4H6 58-59.5 -- -
Cti,CH,-A# CIH,' .59--60
CACHen CjHj, '137-138,5 >" LSO > 150 >150 120' >150 >150 >150 >150 > 150 150
CH.NOg-n CIis. * 118-119.- > J;jO >150 >150 >150 > 150 >150. >150 75. .>M :>150
CjH,OjC-jHrt% CjH&' 93,5.415 >11$O 135 120 00 . >150 >150
1 75
1 150 150
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C4 CA 1 05,5-97
-ACC-NR,AP6031057
Table 3. Toxicity (ng/kg) Of Some COU-
pounds with respect to white mica
compound Mini mim
no. in LDioo LD50 tOXiC
Table 1 dose
11V so 25 12.5
XVI .100 75 25.0 -
The authors thank Professor if. 1. Vashkov for, investigating the toxici
of the preparations fOr MamMals and M. 1. Gagarirtaya for studying the
effect of the preparations on Hill's reaction. Orig. art, has: 3-tabl
SUB CODE: 07/ SUBM DATE; 30a,yW ORIG REF:
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AUTHORS Nazarenko V.A.,Flyantikova,. G'V., Lebedeva...11,Y., 32-8-1/61
TITLE Analysis of Fare Metals. Determiia-tI n of the Arsenic Co4tent,
(Analiz chistykh metallov. Opredeleniye primesi mys9yaka - Russian)
PERIODICAL Zayodskgya Laboratoriya, 1957, Vol 23, Nr 8, pp 891-896(U.S.S.R.)
ABSTRACT Two methods of the separation of arsenic from the bysic metal are
described in the paper, for the purpose of its (i.e. of arsenic)
chemical evaluation. In both cases in recommended the so-called
"universal" type of the separation of microquantities of arsenic
from pure metals on further extraction of the diethyldithiocar-
bamate complex from a strongly acid mixture by chloroform, as
well as the final determination-after the formation of arsenic-
molybdenum-blue in all cases. Then the process of the separation
of arsenic from antimony, vanadium, niobium and silicon is des-
cribed and the use of a siutable apparatus ia demonstrated. In
the case of an analysis of antimony and niobiu* preyious.preci-
pitation of arsenic is recommended is the form of magnesium-am-
monium-arsenate with a phosphate carrier. In-the case Of vanadium
and silicon the separation of arsenic from the corresponding solu-
tions is directly performed.The process of the determination of ar-
senic after t'ie extraction by diethyldithiocarbamate acid is des-
cribed.In thi.3 case a freshly prepared solution of diethyldithio-
carbamihic acid is used for the extraction of arsenic.In that con-
nection it is pointed out that the application of a chloroform so-
Card 1/2 lution of diethylammonium -diethyldithiocarbamate would be more
Analysis of Pure Metals. Det erminat ion of the Arsenic 32-8-1/61
Content.
convenient,but this reagent is at present difficult to obtain.This
method is also applicable to the determination of the arsenic con-
tent ofather matals which do not form any diethylearbamates in
strongly-acid solutions.,neither in the presence nor in the absence
of complex producers.
There are 2 tables and 1 illustration and 5 references.
AVAILjkBLE Library of Congress.
Card 2/2
F t9 F LID E VA
/V, V.
AUTMRS: Nazarenko, V.A., L(~*Dedeva, N.V. , Ravitskaya, R.V. 32-11-V-/
TITLE: The Method of Determining Germanium in Ores, Coals, and industrial
'Waste (Metod opredeleniya germaniya v rudakh, uglyakh i
promyshlennykh otlehodakh) .
PERIODICAL- zavoaskaya Laboratoriya, 1958, Vol. 21+, Nr I , -pp. 9-13 (USSR')
ABSTRACT: In the introduction to this work it is said that the best-kno;a-~ mr--th-
od for this purpose is the phenyl-fluoron colorimetric method. Phe-
nylfluoron (9-phenyl-2,3, 7-trioxide-fluoron) form, a red precipit-a-
tion with the tetravalent germanium in -,,hiich to each germanium atom
there correspond t-ao molecules of the reagent. Various varieties of
this method, in the first line such developed by foreign scientists
like Cluley, Ladenbauer, Slama and Hecht,Luke and Campbell, Schneider
and Sandell, -as well as by the Soviet suientists Gillebrand and
Lendel' and others are cited. It is further mentioned here that T)he-
nylf luoron reacts (like to germanium) also to many other element; of
the groups IV, V and VI of the periodic system. In order to separate
germanium from distufbing elements it is recommended to extract the
germaniLun tetrachloride from the 6-n hydrochloric acid by distillation
or by extraction vrith tetrachloride oirbon from 8-0-n hydrochloric
Card 1/2 acid (examples). In conclusion it is recormended to apply the method
The Method of Determining Germanium in Ores, Coals, and 72-1-2155
Industrial 'Jaste
described uniformly to all materials. A difference in treatment iS
possible solely in the introductory work of separating elements.
This generalized method consists in the extraclion of the genrianium
'th carbon tetrachloride from 9-n hydrochloric acid, .-rith follow-
ing re-extraction .-rlth water and colorimetric determilr"ation -,~rith
pheny1fluoron. A table of results is given -aith re3pect to pyritie-,
copper-, zinc-, lead-, antimony-, and iron ores, coal, coke, and
coal resin. The experimental part of the present 7rork contains three
chapters: "Separation of Samples" , "Extraction and Determination of
Germaniud' , and the "Construction of the Calibratirti, Curve". There
are 411 references, 2 of vrl-"- ch are Slavic.
ASSOCIATION: Ukrainian Branch of the State Institute for Rare Metals and Such aa
Occur in Small Quantities (Ukrainiskiy filial Gosud-arstrennogo in-
stituta redkikh i malykh metallov).
AVAILABLE: Librarj of Congress
Card 2/2 1. Germanium-Determination 2. Germanium-Separation
NAZARENKO, V.A.; LEEEDEVAI N.V.;-EIRYUK, Ye.A.; SIMSTOVA, M.B.
, I MAWANagwor
Complex compounds of multivalent metals with trihydroxyfluorones.
Zhur.neorg..khim. 7 no.12:Z731-2738 D 162. (KMA 16,,2)
(Metals-Anal~sis) (Xantheonone)
5 (2)
AUTHORS: Nazarenko, V. A., LebQdeva, N. V. SOV/32-25-8-2/44
TITLE: Application of Trioxyfluoron Derivates in Colorimetric Analysis
PERIODICAL: Zavodskaya labordtoriya, 1-959, Vol 25, Nr .3, PP 899 - 903
(USSR)
ABSTRACT: The application of phenylfluoron (9-phenyl-2,3,7-trioxy-6-fluo-
ron) (I) for the determination of germanium (II) has the dis-
advantage that the formed complex compound is colloidal. There-
fore,-(Refs 1,2) p-dimethyl-iminophenylfluoron (III) was recom-
mended.as a reagent, as (III) forms with (II) real solutions.
It was established that different 293,T-trioxyfluoron (subsii-
tuted in the 9 Position) derivates can.be more or less used as
reagents for (II)..To establish the suitability of the different
trioxyfluoron.derivates.(TD) for the colorimetric (II)-deter-
mination the molar absorption coefficients of several complex
compounds of (II) were investigated with synthe4ized.. (TD).
The reaction occurred at the optimum acidity of 0-5 n HC1. The
optical density was measured on a Pulfrich photometer at a wave
length of 530 mg. The measuring results (Table) proved that the
sensitivity of the.2~nitro, 4-nitro, and 2.4-dinitro-phenyl-
Card 1/2 fluorons is greater than that of (I). Concerning spectrometric
Application of Trioxyfluoron Derivates in Colorimetric SOV/32-25-6-2/44
Analysis
sensitivity of the reaction disulfopheny1fluoron (u)-surpasse-s
that of II) with the last-mentioned nitro coupounde as well as
that of M. The advantage of (IV) is that the determinations
can be made at a low acidity (from PH 5 to 0.2 n HC1). In case
of strongly acid solutions the use of (I) isj,; ~A preferable
and there also is a possibility that insoluble compounds are
formed with (II) which precipitate. Thus, (II) is most favor-
ably determined by spectroscopy with (IV) in weakly acid so-
lutions (0.02 - 0-05 n-HCI) with the addition of gelatin, while
for strongly acid solutions (above 0.1 n HCl) the (I) and the
above mentioned nitro compounds are to be preferred as reagents.
There is mention of the photometric determinations of Kazarinova
and Vasillyeva, reference 6, which appeared at the time the
present paper was being printed, but which in principle is in
accordance with the presented experimental results. There are
7 figures, I table, and 6 references, 3 of which are Soviet.
ASSOCIATIOM: Laboratoriya Instituta obahchey i neorganicheakoy khimii Akademii
nauk Ukrainskoy SSR (Laboratory of the General and Inorganic
Chemistry Institute of the Academy of Sciences., Ukrainskaya SSa)
Card 2/2
S/073,/62/O28/0O2/oo6/oo6
B1O1/B11O
AUTHORS: Nazarenko, V. A., Flyantikova, G. V., Lebedeva, N. V.
TITLE: Ionic state of germanium in weakly acid solutions
PERIODICAL: Ukrainskiy khimicheskiy zhurnal, v. 28, no. 2, 1962, 266-267
TEXT: The range of existence of oermanium cations in weakly acid solutions
was studied. Experiments were conducted with electromigration and by
determining the germanium content in the electrolyte with disulfo phenyl
fluorone. 0.001 moles of Ge02 solutione in a buffer solution (glycocol,
biphthalate, veronal which do not form complexes with Ge) were filled into
a V-shaped tube with sealed-in platinum electrodes. The upper tube shaft
was filled with the same electrolyte but without Go. Voltage was varied
between 30 and 210 v at a constant amperage of 15 ma. Electrolysis took
60 min. Then, the Ge content both in the catholyte and in the anolyte was
determined. In order to take diffusion into account, blank tests without
current were conducted. Results:
Card 1/2
S/073/62/028,/002/006/006
Ionic state of germanium in ... B101/B110
Ge (pg/ml)
PH in catholyte in anolyte blank test
>7 - only in anolyte
6.63 4-9 6.1 0.9
5-05 4.6 5.0 0.7
3.12 7-7 7.5 1.0
2-32 4.4 3.6 1.1
1.05 1-3 2.2 0.2
Contrary to published data, weakly acid solutions contained germanium
cations in addition to the anions of germanic acids. Their presence
explains many analytical reactions of Ge and aloo their similarity to reac-
iions of other metals of Group IV of the Periodic System. There are
1 figure and 1 table. The most important English-language reference is:
D. A. Ev'arest, J. E. Salmon, J. Chem. Soc., 2436 (1954)-
ASSOCIATIOtf: Institut obshchey i neorganicheakoy khimii All USSR,
laboratoriya v Odesse (Institute of General. and Inorganic
Chemistry AS UkrSSR, Labor.~tory in Odessa)
�UB~I~~ED: September 10, 1960
2
NAZARENFO, V.A.; LEBEDEVA, N.V.
- ----------- ---- ----
Deteriin~~ion of tin in poor ores by p-nitrop-renilfluorcre.
Zav.1ab. 28 no.3:26.3-271 162. (M-IRA 15:4)
1. Instultut AllicheY i neorganicheskoy khimii AN USSR.
(Tin--Anal,,Isis) (Xanthenone)
TIAZARENKO, V.A.; lfIE2F~.IA N.V.; SIMSTOVA, 14.B-; BIRYUK, Ye.A.
,j .- - -.. -
Trihydroxyfluranes. Metrod.poluelli.khim.reak. i prepar. no. 7:
21-24 163, (MIRA 17:4)
L institat obshchey i neorganicheskoy khimii AN UkrSSR, Odessa.
ACCE3SION NR: AP4009727 S/0075/64/019/001/0087/0089
AUMLOR: Nazarenko, V. A.; Lebedeva, No V.; Vinarova, L. 1.
TITLE: Complexometric determination of tetravalent germanium
souRm Zhurnal analiticheskoy khimii, v. 19, no. 1, 1964, 87-89
TOPIC TAGS: complexometric determination, germanium determination,
quantitative je -anium determination, complexone 111, GeO sub 2,
r'n
germanium (IV , germaniiun complex f ormation
ABSTRACT: Complexometric determination of tetravalent germanium in
GeO was accomplished by use of a heated solution of the disodium
sale of ethylenediaminetetracetic acid and a 2.5 fold excess of
complexone M. Changing of the anion into the cation form was found
to proceed slowly, and complex formation occurred quantitatively at a
0.02-0-05 N HC1 acidity. As one mole of Ge02 binds 1 mole of complex-
one, the Ge gram - equivalent is 72.6. The excess of complexone was
titrated off with zinc sulfate and a color indicator. Standard devia-
tion errors were + 1.2% for 15-200 mg Ge and + 4.6% for 0,02-3 mg Ge
Card l/2
ACCESSION NR: AP 009727,
per 50 ml solution. The influence of chlorides on the complexometric
titration was also studied and reported. Complex formation proceeded
nonnally at a 3 mole/liter NaCl content. Orig. art. has: 1 figure
and 2 table3.
ASSOCIATION: Institut obshchey i neorganicheskoy khimii AN USSR,
Laboratorii v Odesse (Institute of General and Inorganic Chemistry of
the AN USSR, Odessa Laboratory)
SUBDEETTED: 27Aug63 DATE ACQ: 14Feb64 ENCL: 00
SUB CODE: CH NO REF SO1,1: 003 oTm: oo6
Card 2/2
CHISTYAKOV, A.D.; BTJRKOVA,,. M.V,.- ORLOVA, Ye.ll.; GLAZOVA. 0.P.;
PEDI, D.A.7, PT-',z-(LYlJTD, 11I.Ye.; ABRAMOVICH, K.G.; POMVA,
T~P.; MATVFYEV, L.T. ; BACHIJAINA, A.A.; -LEBEDEVA, 1U.;
PESK()V, B.Ye. ~ ROMAYOV, N.N.; VOLEVAKil~---- -- - - &ELKO,
.,N.M.; P
I.G.; PETRENKO. f-T IT - WIRNFUNK0. I.V.~ PINUS, N.Z.;
SMAETER., S.H. BATZ-.~;YEVA F-
NININA. L.S.; !EL?SKAYA,
N,N., nLchn.'red.; ZVERE-VA' N:I., nauchn. red.-,
KURGkT,SKAYA, VA~i., naunhn. red.; I-ERTSALOVA, A.h., nauchn.
red.; T011-InAS111HVICH, L.V., nauchn. red, SAGATIOVSKU, N.V.,
otv. red.3 l'l(-'-:'IKOVSKAYA.? A.B..
[1-larmal of short-range weather Rukovodstvc
po k-r-All-oorochgm prognozam pogod,,. Leningrad, Gidro-
meteoizdat, Pt.2. Izd.2. 1965.
(f-lIlLk 18.8)
1. Moscow. TSentralliVy institut pi-opozov.
I
"taoT.1 LaByI)GYA" rv.V.
Chmnf,pu in V:c ctxt--.. -,, wo ct a- -11r, ;~wm. 0-1mg Wic lan6rth if thlo
P-rinta !,A%Ityr in thn Dl~!v-tsm* ucol. 4A1 Lule 6s
153 D-D 165 (MMA 19:1)
1- Subaitted -%y 4j. 1965.
L'318oi-66 ~wvi) RI
ACC NR: Ap6o216772
SOURCE CODE:
AUTLHO11: -Mollnikov, 11. N.; Grapov, _A. Fs; Lebodeva, N, V.
ORG: cientific Rosearch Inslitutp of Chemical Agents for Plant Llro ctio
Q~Enion S -te
Moscov-p (VsesoyuzrWy nauchno-isslodovatellskiy inatitut khimicheskikh aredstv zashchitt
Or
TITL2~; -anic insectorun XCII. Synthesis of acid chlorides, amides, and
anilidoo of o-chlorophorq3jwthylphosphonic acid
SOURCE: Zhurnal obahchey khimii, v. 36, no- 3, 1966, 45o-4-53
TOPIC TAGS: fungicido, insocticido, chemical synthesis, orgarde phosphorus compound,
cheinical bonding, bydrogon bonding, IR spectrum, toxicity, organic amide, chlorinatedi
organic compound
ABSTPa%CT: Derivatives of 0-3-chlorophenYl- and 0-4. chloraphonyl-
methylphosphonic acids were synthesized in a search for new insecto-
fvngicides, on the basis of the theory that the Insecticidal properties of
.the preparations increase with increasing acidity of the acyl radical boLmd
tothe phosphorus atom. Amides and anilides of 0-3-chlorophanyl- and 0-4-
chlorophony:Lmothylphosphonic acids were synthesized by the reaction of the
chlorides of these acids with primary and secondary amines or substituted
anilines, The formation of intermolucular hydrogen bonds in the
Aialkylamides was suggested by their low melting points and infrared spectra.
L 318ol-66
ACC NRs AP6021672
BI,olo'i*a1 ti-ato indicated high insecticidal activity of the prep~aratibnsv-
A g 0
oome exhibij~ad herbicidal activity. Orig. art. has: 1 figure and 2 tableo. CJPR33
SUB CODE t 07, o6 / SUM DATE: 3-1 Feb65 / ORIG IW- Ft 003
t ~,
Card '4
-L 314 khA 34T(1) RO
ACC NiZi SCU--ZE C002;: G?.70079'1667o36/co3lc4,c7lc-';.;~,:.~..'
AtE?-TOR: Vallvakov, No Noj Griipcv, A, F#t Lootwlovn, 11. V.
ORG: 4M-Union Scientific Rosekrch in
(Vv,osoyuisayy nauchno-isslodovatellsklLy
rastarzdy)
sxvdsty zashchlity
~x
TITU.':-, Orgwiic insnqtofw~~Icidas WIV. Arddes o-L O-arylx-vthvl- and clUoromthyl.-
phosphonic acids
Zhurn.,LL oWhchoy IdArIdi, v. 36, no, 3, 1966, 457-461
OPI- C T,
T
AGS: fungicide, insecticide, phosphon:ic acid, organic a=ido, chardeal
synthosis, chlorinated organic compound, plant develop:mnt, to'deity
A series of amides of O-arylmethylphosphonic acid were synthesized
by reaction of N,9-&alkylamidomethy-lphosphonic acid chlorides with phenols
;in the presence of triethylamine. N,N-diethyl-S-4-chlorophanylmathyl-
I:thiophosphonate was synthesized analogously. O-Arylmothylphosphcnic acid
,chlorides wore found to be stable o�ly when the original phenols have an
ionization constant less than 1-10- . Otherwise the chlorides are unstable
and are readily bydrolyzed in air to 0-arylmothylphosphonic acids.
O-Arylehloramethylphosphonic acid smides vmrs synthesized by the reaction of
-0-ary1chloromethylphosphonio acid chlorides vith amines. The compounds pro-
L 31813-66
ACC NRs AP602'
I
duced exhibit substanitial herbicidal activitys in &__concentration of 1-15
- _grg of radish routs.
-parts per mllllon,th~yyi~~uce 50% inhibition of tl;e wt4 Bp; .
.&n4 roots-, A. V. Buzovk'm Participated in the experimental part of the work.
Orig. arte M: 2 able s ~. ~~7
Sn CMEI 07, 06 / SUEM DAW: 15FOb65 / ORIG REF; 005 / OTH REF: 005
/
I I
is 0 0 a 0 0 0 e 0 0 0 0 0 0 0 0 0 9 0
11A
6, -0
0 4 's,
0 0 0 0 0 0 0 0 41 0 0 0
L"
AI-L-A r f a M LLY z
1 9 L a N-r--Q~ R-A-1-k-y-
0
41, A !$- A- 1~
Ar q-.
Studies on the blfiu*ftc* of seft" reaction nzodiA aa cho
*C6011 Ot SUCCOC41- X. VA-1XbVkYA LStAIV9FAJ %Ie,1-
'
Z
oksiAol. 9, NUA, 0-121;1916).-
:-so
In M-Arch of Causes for tntm~i"tiun by Acidity,
and
40 wr4kenhil by alky., e1jects of 9 nimAk, w"e I et,,I j~n
: i-Aal"I I" heart. pcrfu~cd with Rinser solo. buffemi
0 with N&11101~ to 3 pit tevvtt (d.4, ",m, atut 1,he
46 i tests TCvt*I;! groUPS 0( OBJMCAks: C11LI, n&tV%AAn. HW.
trional and urethan showed no sensitivity to pit. su-
hital. pbenobatbital, and aytal "ere quite sensitive
i
10 Pit, reaching Malt. AOMtY of, Ifie acid side. Thuq, Moo
,
'
j phenobabital (JAXO) decrr"-d "MIAC amplitude W.
il
=eo
; ,
t 411, And 7%~ at pit 11.4. 7.0. an-I 7.8; the nwr"Ijing
'
:W:)
k)
fi
ffl
1
:,izo
gmet at
:
were I
, and 19
;- Sensitivity
, 1 t
W 1111, %hown by h2thitUfAtrs hUt not by 41111er Ufrtifiei_
-
6 Att
ih
1
1
1
4
i
T as*
to
,00-en-
l
"
0
Ulittimer
vit.
w tests con.
he
alkAli
go*
00-4 a**
Pharmacology Lab :;99
.
p4
ties,
A 111
ALLLF.(,KAL LIURAILRE CLASSIFICATICh !Moo
S:
&s0
A'
I ~U ;
t 19 Is at N 9 it 9 it it if or
A3 a 3 4
0
n 1 ;1.
9
't 00 0 411 a *is 411 0 41 0 0 9 0 0 * 46 * 0 0 * 0 !Q a 0 0 a
A
00 *a* Oleo 0 0 0 0 0 * 0 0 o o 0 *--4 o is so 0.0 o a o o *so* o
: : so"
7-58-11-5/15
AUTHORS: Khitaroy, 11. 1., Rengarten, Ye. V., Lebedeya, 11, Ye,
TITLE: The Chenical Composition of Liquid Inclusions in Iceland
Crystal and the Problemsof Its Genesis 0[himicheskiy sostav
zhidkikh Yklyucheniy inlandskogo shpata i voprosy genezisa)
PERIODICAL: Geokhiviya, 1958,, Nr 3,, pp. 214 221 (U3SR)
ABSTRACT: a crystals from the
KiTeylenko and ff~N. AjidruG(~iit--o~ They are fron. four differc,',t
tapes of deposits-,
1 Gonchak and Nidym deposits- 2)Shpat depos-itt. 3)Yangurakta
and Kuktule deposits, 4)Dzhek-iride and Markhays. deposits.
The content of 00 2 and water of the vacuoles was deternined
in a special apparatus whi:~h is given and described in a
schematic diagram; the device for opening the vacuoles is shown
in a figure. The salt contents were determined by means of
microanalysis. All results are compiled in a table, The second
part treats the particularities of the composition of inclusions
Card 1/2 and the conceptions concerning the genesis, The inclusions con-
The Chemical Composition of Liquid Inclusions in 7-58-3-5/15
Iceland Crystal and the Problenslof Its Genesis
ASSOCIATION:
SUBMITTED:
sist of rather concentrated solutions of chloride,, calcium,
and sodium. In order to be able to fix the hydrothermal for-
mation conditionsr. it waa tried tc wash out gabbro-dolerite
(Dzhekindin deposit) by means of water, NaCi- and CaCl-- so-
lutions under various conditions~ The results are shown in two
tables and one diagram. Hence results a for-nation temperature
of the crystals of below 2oaO at a. pressure below 15-16 atmos-
pheres; the low CO 2"' content as we!.!. as the conplete development
of the crystals speak in favor of this Iorte-p-rature, There are
5 figures, 3 tablesiand 2 references., 2 of which are Soviet,
Institut geokhiriii i analiticheskoy khimii im~ V.I, Vernadskogo,
AN SSSR~ Moskya ( Moscow Institute of Geochemistry and A-naly-,
tical Chemistry izieni V. I~ Vernadskiy,AS USSR)
March 5~, 1958
L -: ties Galcit~a crystals.---
Cal~Ata ~rystals-impur_'
Temperatura fat;~crs 3. Chamical
Salts- -Determizzati%yi
Card 2/2
HWM)
'AA(t. Nil-i` 1JR/0216/65/000/0410507/05
20,
577,*391
~AUTHOR: Y&zJLnj Aq M,; P1 shevskaya. Ye. R-.; 1~0-1 V*A
;Ivanitakaya. Ye. A,; LebedeXA1 W, Ye.: K om T.
Tokarskayaj S. M K.---
MITLE: Role of the "orthophonol-orthoquinone" s7stem in the
iprimary mechanisms of radiation effect on the.organism
ISOURCE: AN SSSR. Izvesti-ya. Seriya biologichealca7a, no, 4* 1965,
'507-520
!TOPIC TAGS: radiation biologic offect,,,phonols quinone,, enzyme,
desoxyribonucleic ac,id., tyrosine.9 oxidation
-A
ABSTRACT: A hypothesis stating that the oxidation reaction of
lorthophenols in response to high energy irradiation is closely
.related to.the formation of orthoquinones (somi(juinones) has evolved
~ f" om
i
fi, the experimental work of the laboratory with which the authors
!are associated. In the present study the immediate effects of
!Z-irradiation on enzyme process rates were investigated in a
ltyrosine+tpos-Inase model system under strictly controlled conditions
I Card
ACCESSION MR: AP5017763
J210 kvP15 mar no filter, 100 to 1000 r doses., .10 min incubation).
'Change in enzyme process rate was determined by the concentration of
newly formed orthophenols, and orthoquinonese With irradiation of the
-,:whole systemp the concentration was 5 times higher than for controls,
-.Irradiation of only the tyrosine solution led to a lesser eoncentra-
Itiong and theconcentration decreased still further with,irradiation
~of only the tyrosinase, When the irradiated mixture was.incubated
i
with a suspension of mouse thymus nucleis the tyrosine oxidation
products, (orthoquinones) were completely absorbed by the nuclei.
;F
luorescence. tests with acridine-orange on thymus nuclei of mice
Immediately after irradiation and tests on thymus nuclei treated with
i
ityrosine oxidation products demonstrated the similarity of irradiatior
I
:effect and orthoquinone effect. The same effect was demonst~rated
with quinone extracts from gamma-irradiated plant tissue (potato).
I
;Treatment,of carbon-labeled plant sprouts with extracts from irradia-
Ited plants depressed DNA synthesis by 50 to 60%9 the same as atter
'gamma-irradiatione Injection of purified orthoquinonesp extracted
:from irradiated plant tissues,,~into young mice caused loss of weightp
"Ilrowth inhibition# and a sharp decrease in leukocyte level of the
.,peripheral blood@ These study data demonstrate the importance of the
L 25811o-66 EWT(I)/EWT(m)/T JK
ACC NR: AP6015925 SOURCE CODE: UR/6216/65/000/OW0507/0520
AUTHOR: Kuzin, At M.; Myshevskava. Ye. -Plyshovskiya, E. G.; Kopylov, Ve A#,
Ivanitskayai Yoe_,A.~i~vanitzkaya, Pe A.: &9bodgy-as go- ;01-16bodevaTT. E.;
Kolomi3,tseva, I* Ke--Kolomiytzeva, I. I.;-- l'nik64t,-S* Ko_41olnikova, So Ke
Tokarskaya, V.I..
ORG: Institute of Bio&sics. AN SSSR, Moscow (Institut biologicheskoy fizik! AN SSSR:
TITIB: Function of the orthophonol-orthoquinone system in the early mechanism of
action of ionizing radiation on the organism
I ri
SOURCE: AN SSSR. Izvestiya!.f Seriya biologicheskaya, no* 4. 1965. 507-520
TOPIC TAGS: ionizing radiation, radiation biologic effect, radiation plant effect#
tyrosine, sorption, oxidation, DNA, biosynthesis, radiation sickness
ABSTRACT-.. 'Ifie- ad1ho'ig_'c6iidu_ded from i-4'airi-lety. -of 7_e)iperfrWnts- o.n-plan ts
and-anImals that the Initial processes In the irradiated organism develop
In the following sequencet
1 (1) During Irrad.Lation the formation of active radicals causes very
slight radiochemical oxidation of the phenols present In the cell, chiefly
tyrosine~
(2).The resultant oxi-1-ition products activate tyrosinases which
Jimmediately after.irradiation leads to the formation of large quantities of
ibiologically.active~%rthoquinones.
(3) 1he.resul.tant orthoquinones are actively sorbed ~y_the_ cell nuclei@:
UDC: 577.391
L 25811-66
ACC NR, AP6015925
0., inzh.; ROZOV, R., inzh.; TYUISNEV, V., insh.
High structure for a seismic district. From. stroi. i inzh.
soor. 4 no.3:43-41+ My-Je 162. MRA 15:7)
(Barauni~ India-Petroleum coke)
(Earthquakes and Wilding) (MIding, Iron and stsel)
04
ACC NR.
AUTH':r%.:
U V"
AP661-l"570 SOURCE CODE: UR/0051/66/020P)3/0503/0505~!
Gryaznov, Yu. M.; Lebedev 0. L.; Chastov. L. A.
ORG: none
TITLE: Passive Q-switching of a ruby laser with bleachable phthalocyanines
SOURCE: Optika i spektroskopiya, v. 20, no. 3. 19669 503-505
TOPIC TAGS: ruby laser, laser R and D, phthalocyanine
ABSTRACT: The application of reversibly bleaghable phthalocyani~e solutions for.
-generation of-giant -pulses from a ruby laseAras the subject of several
'previous Soviet and American studies. Phthalocyanines'of magnesium,
vanadiun-~ zinc, copper, and metal-free phthalocyanine in pyridine or
quinoline solutions were previously used by a team of Soviet authors headed
by V. N. Gavrilov and Yu. M. Gryaznov [association unknown] to generate
5 UDC: 621.375.9:
L o4643-67
ACC NR: AP6011570
shingle pulses of 1 Mw maximum power from a ruby laser. Another team
.o f Soviet scientistr:~ headed by A. L. Mika2ly-an, obtained pulses of less than
20 nsec duration from a ruby laser employing a vanadium phthalocyanine
,solution in nitrobenzene-,.as a passive Q-switching element. A third Soviet
iteam, composed of L. S. Dovger, B. A. Yermakov, A. V. Lg!Ldnand L. P.
Shklover, in a study of bleaching of certain organic solutions in the cavity
of a ruby laser, found the efficiency of vanadyl phthalocyanine in nitrobenzene
'and kryptocyanine in methanol was- nearly equal in generating giant
*pulses; the efficiency of zirconium phthalocyanine solution in a-bromo-
naphthalene was several times lower. To the present time, the best
results were obtained in 1964 by a team of IBM scientists with a solution of
aluminum phthalocyanine chloride in 1-chloronaphthalene.
Recently, the above-mentioned team of Soviet scientists headed by Yu. M.
Gryaznov published the results of a systematic study of some 22 phthalocyanines
and naphthalocyanines. These scientists attempted to expose the relationship
between the energetic characteristics of giant pulses and spectral absorption
properties of Q-switching solutions of the phthalocyanines studied. Only
fifteen most chemically stable compounds were considered in the study with
the apparent purpose of selecting the most efficient of them. Quinoline and
o-dichlorobenzene were used as solvents. The total energy output of a
Lo4643-67
ACC NR: AP6011570
series of giant pulses and the average energy output of a single pulse were
generally increasing with a decrease in the difference 'between the wavelength
of maximum absorption of the compound and the 6943 A wavelength of laser
emission. This conclusion was made from a comparison of the data presented
in Fig. 1 and the wavelengths of maximum absorption of the compounds, which
:-are, respectiiely: I - 6925; 2 - 6910; 3 - 6880; 4 - 6900; 5 - 7020; 6 - 6800; .
7 - 7060 A. A shift in the position of maximum absorption toward the 6943 A
emission line in the sequence: Cu `- Al "' Cr I Ga of the phthalocyanine series
coincided with an increase in the emission output of the laser. The A max of
absorption also shifted one way or another when O-dichlorobenzene was
substituted for quinoline as the solvent.
The best results were obtained with gallium phthalocyanine chloride and
zinc naphthalocyanine. Performance of the gallium phthalocyanine chloride
solution' in quinoline as the passive Q-switching element in a ruby laser was
illustrated by the following data. Single pulses of -18Mw power output and
-40 nsec duration were obtained at 0. 7j energy of a pulse (2076 of the. energy
output in the tree mode generation of the laser) from an 800 mm long cavity
containing a 120 mm. long ruby rod between the mirrors with 50 and 99% reflec-,
tion. Width of the emission spectral line was narrowed to less than 3 -10 2 A
when a bleachable solution was used.
Card 315
4C NVRt-- XAOMWO
PPV-
Pli
b
M a
aio -
4
0.8-
0.8- 5 0.05-
03- 7
0 .44 M UY 2.0 ?..1
:Fig. 1. Pump energy (w) dependence of the total ener&7 output (P) of a series
tof giant pulses (a) and of the average energy (Pav.) of a single pi~lse (b) with
.-certain bleachable compounds.
I - gallium phthaloc)anine chloride; 2 zinc naphthalocyanine; 3 - chromium.
phthalocyanine chloride; 4 - copper naphthalocyanine; 5 - vanadyl phthalocyanine;
6 - copper phthalocyfnine; 7 -.kryptocyanine. Solvent: quinoline. Cell
transparency: 60%.
Card
L 04"47;-617
ACC NR: LP6011570
L/
A study of the effect of transparency (concentration) of the gallium
phthalocyanine chloride F,olution on the energy output of a single pulse
indicated a maximum energy ( -0. 75j) at about 207a transmission. A decrease
in the energy output wita decreasing transparency below 2076 was attributed
to a lowering of the cavity Q because of absorption of energy of a giant pulse
by the phthalocyanine molecules in the ground and excited states.
In condusicn, the authors thank V. K. Kolesnikova, V. N. Gavrilov, and
V. V. Kozlov for assistance.
COMMENT: A limited search of the Soviet literature published in 1964-66
failed to reveal the association of the authors of the article reviewed, The
association of the other Soviet scientists mentioned in this mte could not be
i ascertained at the present time. However, other sources indicate that in
~965,1,. P. Shklover was associated with the All-Union Institute of Chemical
:__a!jagEijts and in 1963, withthe Moscow Institute of Fine Chemical Technology,_
Information published after the -r--e-v-ie--we-da-rtic1e -~ 5nfimt~her Sovietyrogress in
Lhe application of phthalocyanines in tjjc- passive-seritefied ruby-lasers ittas
reported in the ATD Press.
Orig. art. has: 2 figures and 1 table.
SB: v. 2, no. 101
SUB CODE: 20 SUBM DATE: NJul.65: / ORIG RET : 002 / OTH UP,: 003
i Card 5/5 ~""a
LEB7,T)TIA, 011pa Aleksandrovna
D -- 7 u
ynAmics of Blood Clots of Children r.,f Epri, Age ConcerninF Acute
Opstric Diseases of the Bowels with Toxical (sindromom)
Dissertation for cindidate of a -ca I-Science deFr(-e. Chair of Pedintrics
( T"r-of. P.A. Byreyev) Saratov Y-dicq! Institute, 1