SCIENTIFIC ABSTRACT AKIMOVA, L.N. - KUZNETSOV, V. I.

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• Document Release Date: June 5, 2000
• Sequence Number: 4
• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

AKIMOVA, L.N.; KIRYUKHINA, Z.V. [deceased].
Protein microstructure models. Part 2: Preparation of
N-aminoaoyldiketo-
piperazines from imino-ester (o,o-dibenzvl-2,5-dihvdropyrazine).
Zhur.ob.khim. 27 no.7:1917-1921 Jl 157. (MIRA 10:10)
l.Moakovoldy gosudaretyennyy universitet.
(Piperazine) (Pyrazine)

fy)c ItIll
-AK Novi,. L N - GAVRILOT, N.I.; AXIMOTA, A.A.
On some proportion of 1-bensylated peptIdes. YArt 2. Zhur. ob.
khim. 27 no.8:2268-2973 Ag '57. lor-9
1. Ylloskovskly gosudaretvenW pnivereltat.
(Ppptides)

AUTHORSs Vovehanko,G.D.# Gavrilov,N.I.,and SOV/55-58-1-1/33
Akimova,L.N.
TITLEt The Albumen Pro'jlem From the Point of View of Modern
Sciences
(Problems, belka v evete nekotorykh dannykh eavremennoy nauki)
PERIODICALt Vestnik Moskovskogo universiteta, Seriya
fiziko-matematicheakikh i
yeatestvannykh nauk, 1958, Nr 1, pp 3-22 (USSR)
ABSTRACT3 The paper given a detailed survey of the modern
state of research
of albumen. The albumen problem in denoted to be the central
question of philosiphy and natural sciences, where numerous
extracts from the "dialectics of the nature" of Engels as well
as
several citations of Lenin shall certify this point of view. In
connection with the poiitical tendency of the article is.the
special consideration of the Soviet research of albumen. The
authors
mentions Zelinskiy,N.D. and his school (chemistry of amino
acids
and other products of the albumen hydrolysis),
Gavrilov,E.I.'(form
of albumen molsoules~, Talmud,,D.L. (legalities of the
structure
of globular albumens , Kargin,V.A., Vilenakiy,V.A. (physical
chemistry of albumetne), Belozerskiy,A.N., Prokoflyev,M.A.,
Manipylov,S.Ye.(nualeoproteids), Kedrovskiy, B.V.,
RumyantsevfA.V.9
Card 1/2 Naeanov'D.N. (morphology and physiology of the
cellular structure

The Albumen Problem From the Point of View of Modern Sciences
SOV/55-58-1-1/33
of albumens), Engellgwrdt,V.A., Lyubimova,M.N.(demountirg of
albumen in muscles), Pavlov,I.P., Danilevskiy,A.Ya., Bakh,A.N.,
Blagoveshchenakiy,A.V. (ferments and their synthesis),
Pry&ajshwtkoT
D N. (change of nitrogen of plants), Orekhovich,V.N. (cellular
aibumen), Konikova,A.S., Kritsman,11.0. (changes of albumen as
a carrier of life).
There are 48 references, 31 of which are Soviet, 2 Swiss, 8
German,
5 American, 1 Italian, and I Swedish.
ASSOCIATION:Laboratoriya khimii bolka imeni akad.
N.D.Zelinskogo (Laboratory
of Albumen Chemistry imeni Academician N.D.Zolinskiy)
SUBMITTED: August 2~9, 1957
Card 2/2

X

79-2-206/64
AUTHORS:
Akiraova, L. 1.1. , Yuranova, 1. P. , Gavrilov,
IT. 1.
TITLE:
On the Models of Protein Microstructure (0 mode1jakh
nikrostruktur

bd-ka) III. On the Structure of
Phenylalaninanh.',rdride Dcrivatives

(111. 0 strukture proizvodnykh
fenilalaninangidrida)
PERIODICALt
Zhurnal Obshchey Kbimii, 1950,
Vol. 26, Nr 2, pp. 398 - 403 (US3R)
ABSTRACT:
In the preceding
report it was shovin that the formation of 11-auino-

acylderivatives of phenylalaninanhydride takes place especially

smoothly and with a Cood yield, when the phenylalaninanhydride is

acted upon bj chlorine anhydrides of anino acids (reference 1).

Formerly, in the investigation of the behavior of If-ai.'Iinoacyl
deri-

vatives of Clycine anhydride, their extrao:odinary stability
ir4an

alkaline Liedium and a peculiar behavior toward the influence
of

hydrazine were eiiphasizod (reference 2). This resulted in the
fol-

lowin',: 1) The addition of hydrazine to the CO-Groups of the
phtha-

lyl protection in the performance of the reaction in the
cold in

etber or alcohol; 2) the splittin., off of the phthz,.lyl
.-roup on

heatin.- in alcohol and 3) the splitting; of the dike to
I)i 1)era,.!ine

rinA with the forwtion of
phthalyltripeptide-lVdrazide, without a

breaking of the acyl bond.
In the present work the properties of

the phenylaluninai-ihidride
derivatives vrere investi-ated and their
Card 1/4
easy hydrolyzation
under the influence of aqueous and alcoholic

70-2-06/64
On the Models of Protein Ilicrostructure. III. On the Structure
of Phenylalanin-
anhydride Derivatives
alkali-solutions and hydrazine .-ias shown. Thus the influence of
the aminoacid composition, as .ell of the anh.;dride as of the
acyl
.-roup upon the properties of these derivatives was for the first
time observed in the example of the aminoacyl derivatives of two
anhydrides (alycine anhydride and phenylalanine anh.;dride). The
in-
fluence exerted by the aminoacid. composition upon the stability
of
the 11-aminoacyl- as well as the acyclic bonds was noticed in the
in-
vcstigation of the properties of the aiminoacid. anhydride
derivati'as
synthesized by the authors. It was foun] that the stability of the
cyclic bond in aminoacyl anhydrides is not,only depandent on the
aminoacid composition of the anhydride but also on the ainino
acids
which are contained in the amine-acyl-side group. In contrast to
U
the easily decoi.-LposinG autinacyl derivatives of
phenylalaninanhy-
dride the same Glyoine anhydride derivatLves (according, to their
aminoacid composition of the awinacyls) are extreimly stable. Thus
the stability of the NH-CO-linka~;e ii different in an isolated
cycle and in a cycle with the IT-auinoacyl linkage and depends on
the ataino acids vibich are contained in the cycle ol t,,,e
aminoacyl
~;roup. The stability of the 11-acyl- ar,d N-auinoacyl linkages
di-
U
rectly depends on the aminoacid conposition of t1)e anhydride. It
Card 2/4 becomes e'specially obvious in the inveati-ations of the
inbraction

79-2-26/64
On the Models of Protein Microstructure. III. On the Structure
of rhe.-11--lalanin-
anhydride Derivatives
1 1 n
products of the anhydride derivatives with hydrazine. The
IT_U::i 0
acyl form of the linkcage, as one of the cheraical compotind3 of
di-
kctopiparazine with amino acids and their derivatives, connot be
investiGated separately$ isolated froi-.i the amino acid3 which
parti-
cipate in their formation. 3u,x,iary0)12hc of tht N-aplino-
acyl derivatives of the phonj1alaninanhydrides -iias dZueribid:
11,111-
-di-phthalyl -lycyl- and
N,l~ll-di-plit)Laljlulanyl-l)li,!n,,l--,lanrlanliydri-
de. 2) The earlier expresied assumption on the mecllanian of tbc
elimination of the 11-aminoacyl ~,roup from these con-pounds
undor
the influence of hjdrizine %was confirmed. 3) The authors
invc3ti-
,3nted their behavior tinder th2 conditions of the b-Juret
reaction
of protein (A % NaOH). The authors shorted their decorl]0osition
under
the influence of alkali, to
plithiloyl-lycyl-plien,rlalanyi-phenylala-
nine and phthaloyl-alanyl-I)henylalanyl-Inhenylilanine. 11) On
the
basis of titration values (according to Villshtetter) a decoopo-
sition scheme of 11-Ni-di-phthalylvalyl-phanylalani-ne anhidridc
tinder the influence of alkali was au-~;ested. There are 1
+.~,ble,
0
Card 3/4 and 4 references, -all of which are Slavic.

On the Models of Protein Microstructure.
anhydride Derivatives
79-2-26/54
III. On the Structure 02 Phenylalani-n-
ASSOCIATIO11% Moscow Mte Miye;rsitY.-
~;usudarstvaniy,,~ nniveroitet)
SUBMITTED: JanuarY 7, 1957
AVAILABLE- Library of Congre3s
Card 4/4

AXMVA...IA-
Diketopiperazines, structural elements of the protein
molecule
(diketopiperzine theory of protein structure).
Khim.b4lla no.l:
35-88 161. (Proteins) (Piperizine) (MIRA 15:1)

ARIMOVA L N--
Bonds formed between tliketopiperazines and amino acids.
Rhim.belka
no.1:89-140 '61. 04IRA 15:1)
(Prote.l.na) (Piperazine) (Amino acids)

AKIMOVA, L.N.
Fermentation of diketopiperazines. Khim.belka
no-1:245-255 161.
(MIRA 15:11,
(Piperozine) (Fermentation)

GAVRILOV, N.I.; GRIGORIYEVA,, I.P.~-, ~MOVA,_L.N.;
YEROKIIIN,, V.K. (deceased]
Certain properties of trityl peptides. Zhur. ob. khim.
31 no.3:739-
742 Mr 161, (MIRA 14:3)
1. Moskovskiy gosudarstvennyy universitet.
(Peptides) -

207-42
S/020/61/137/002/016/020
0 a B103/B215
AUTHORSt Stesik, L. N., Akimovaj L. N., and Apin, A. Ya.
TITLEt Determination of the width of the reaction zone, and the
parameters of the detonation wave of a comDact exDlosive
PERIODICAL. Doklady Akademii nauk SSSR, v. 137~ no. 2, 1961,
369-371
TEXT: The authors measured the width of zone a of the chemical
reaction
and detonation wave of a compact explosive with practically
optimum density
(1.58 9/cm 3), namely H (N) ballistite powder with a
nitroglycerin content of
approximately 27%. The charges had a diameter of 40 mm and a
height of
'00 mm. The powder wa2 fired by a lensehaped charge
guaranteeing a plain
detonation front. The detonation velocity was 7010 m/sec. The
zone width
iEi the distance between the front of the shook wave and the
Chapman-Jouguet
p'.ane. The authors determined the zone width by the methods of
R. Duff,
E. Houston (Ref. 1: J. Chem. Phys., ?J, 1263 ~1955 )and A. N.
Drimin,
P, F. Pohkil', (Ref. 2i D01, 127, no. 6, 1245 00.5fl), in which
first the
shaDe of mass velocity u is determined by an aluminum plate
moved by the
Card 115

20742
Date.rmination of the width S/020/61/137/002/016/020
... B103/B215
explosion. 1i the shook aiiabatic of the metal, and the detonation
velocitJ
are known, a cm be calculated from the'formula
b (D - V) (u + c - DI) (1),
DJ(u + 0 - V)
where b denotes the thickness of the metal plate, at which a
discontinuity
on the curve u = 1(6) occurs; D is the detonation velocity, D 1
the average
velocity of the shock wave in section b of the metal, V the
average velociv
of the moving boundary between explosive and metal, u and c
velocities of
mass and sound in the metal with a depth of b. The discontinuity
of curve
u - ~(J) (~ - thickness of the metual) has been experimentally
proved. The
mass velocity of the metal at this point is determined by pressure
and
mass velocity of the detonation products in the Chapman-Jouguet
plane of
the detonation wave. The authors used 0.3-5 mm aluminum plates,
whose shock
adiabatic was known. Table 1 and Fig. 1 give the experimental
results.
The values of mass velocity of the aluminum adjacent to the powder
was
Card 21b"~

207h2
S/020/61/137/002/016/020
Determination of the width... B103/B215
calculated from the known shook adiabatics. The authors found
the
discontinuity of the curve u T (6) to occur at a plate
thickness of
0.85 mm. D 1 - 7520 R/sec, V : 1730 M/sec, u = 1360 m/sec, c =
7590 m/sec.
Hence, a reaction zone width of 0.12+0.4 mm was obtained. In
formula (1),
however, the rebound of the detonation wave on the boundary
between ex-
plosive and metal is not taken into account. The authors
determined the
width of the non-disturbed reaction zone of powder N on the
basis of the
function of Ref. 2 which gives the relation between the
measured value of
a and the dynamic rigidity of explosive and metal (the dynamic
rigidity is
the product of initial density and velocity of the shock wave
(?OD)). The
above width is 0.15�0.5 mm, On the basis of their experiments,
the authors
determined the polytropic curves of the detonation products
(for method of
calculation see Ref. 6s A. N. Dr8min et al, DAN, 128, no. 5,*
989, 1959):
P = 2.4-101 Oy2_ 80 bar (2). The values characterizing tYe
state of the
substance in the Chapman-Jouguat plane are: P - 204-10 bar, y -
2.14 g/cM11
0 = 5160 m/sec, u = 1840 M/sec. Since the average value U in
the reaction
zone is 1.25 times as high as u in the above plane.. the
authors calculated
Card 3AY

20742
S/020/61/137/006/016/020
Determination of the width... B103/B215
the duration o! the chemical reaction of powder N in the
detonation wave as
follows: t - a/(D - _U) - 3.3-10-asec. According to their
calculations,
the critical diameter dcr of the powder N is 28 mm. They proved
d or /a to
be approximately 200. Since the detonation velocity of compact
powder does
not depend on the diameter of the charge, critical and ideal
velocities
practically do not differ. Hence, the authors conclude that the
detona-
tion vanishes without ejecting the incompletely reacting
substance from the
reaction zone. This vanishing is caused by radial expansion of
the detona-
tion products occurring along the edges of the charge. It is
known
(Ref. 8, H. Eyring, R. Powell et al., Chem. Rev. '. _42, 69~
1949) that the
detonation front is bent due to this expansion, i.e.9 the
smaller the
radius of the charge, the more it is bent. The current of
nubstance is
diverged when passing the bent front. This means that the radial
expansion
of the substance behind the front of the convex detonation wave
covers the
whole cross section of the charge, irrespective of the distance
covered by
the dispersion wave. A certain curvature of the front causes the
pressure
to decrease to an extent which stop8 further expansion of the
detonation.
Card 4/8
5'

20742
81020161'1137100610161020
Determination of the width... B103/B215
There are I figure, 1.table and 10 references: 8 Soviet-bloc.
''ASSOCIATIM Institut khimioheskoy fiziki Akademii nauk SSSR
(Institute
of Chemical Physics of the Academy of Sciences)
-PRESENTED: October 29, 1960 by V. N. Kondratlyev, Academician
SUBMITTED: October 26, 1960
Card 5/f

197 0
GOFMANt A.; FREY, A.I.; RUTSHWN, I.; OTT, Kh.; SHEMYAKIN, M.M.;
KISHFALUDI,
L.; KOCHETKOV, N.K.; DEREVITSKAYA) V.A.; FROKOFIYEV, MA,;
SHABAROVA, Z.A.; FILIPPOVA, L.A.; SHANKYM, S.; KHAYGA, S.;
LIVI F,; ROBERTSp M.Ye.; GAVRILOVt N.1.1 XWMI-~1 KRLUDOVA,
H.S.; WSIWVp V.I.; IZELINI B.M.; SHEPPARD, R.K.; WODINSKAYA,
Ye.N.1 VASINAp O.S.; BERLIN, A.Ya,; SOFIINA, Z.F.; 1ARIONOV,
L.F.;
KNUNYANTS~ IOL.; GOLUBEVAt Nje.j KARPAVICHUS, K,I.j KILIDISUVA,,
O.V.; WDZIMMY, X.1 KAFTAR~ H.; LEV, M.; KORENSKI, F.;
BUASSONAp R.A.; GUTTMAN, St.; KHOYGENIN, R.L.; ZHAKENO, P.A.;
BAZHUS, S.; LENARD, X.1 DUALISKI, S.; SHREDER, Ye.; SHMIKHEN,
R.;
KHOKHLOV A.S.
:f
Results
the Fourth European Symposium on the chemistry of
peptides. Abstraets of reports. Zhur. VKHO 7 no.0468476
162. (MIRA 15:8)
Aktaionernoys obahchostvo "Sandos", Basalt, Shveyteariya (for
Gbfkoan, Frey, Ott, Rutshmann)... 2. Farmatsevtichaskaya fabrika
"G.Rikhter", Budapesht, Vengriya (for Kishfaludi, Korenski,
DuAlski). 3. Institut khimii prirodpykh sojedinenly AN SSSRp
Moskva'(for Kochetkov, Derevitskaya,.8h4ayakin, Khokhlov).
4. Labor"atoriya khimii belka Moskov6i6go gosudarstvennogo
universiteta (for Prokoftyev, Shabarova, Filippova, Gavrilov,
Akimova, Khludova). 5. Fond meditsinskikh issledovaniy,
Paseadena,
Kaliforni a, Sev.Soyed.Shtaty Ameriki ffor Shankman, Khayga,
Liv,
Roberts). 6. Laboratoriya khimii belka Instituta organicheskoy

AMOVAI L.N.; KORSUNSKAYA, L.O.
Effect of the combined protection of aminegroup in
peptides on
their properties. Zhur.ob.khim. 32 no.9:2809-28:L2 S
162.
(KA 15 -.9)
1. Moskovakiy gosudarstvennyy universitet imeni M.V.
Lomonosova.
(Peptides) (Amines)

PONOMAREV, V.V.; ALEKSEYEVA, T.A.; AKIMOVA, L.N.
Heats of combustion of some peptides. Zhur. fiz. khim, 36
no.4:874"-873 Ap 162. (MM 15:6)
1. Moskovskiy gosudarstvennyy universitet imeni Lomonosova.
(Heat of combustion) (Peptides)

PONOMAREV, V.V.; ALEKSEYEVA, T.A.; AKIMOVA N
- , L. .
Heats of combustion of some anhydrides. Zhur.fiz.khim.
36
no.5:1083-1085 Fq 162. (MIRA 15:8)
1. Moskovskiy gosudarstvannyy univeraitet imeni
Lomonosova.
(Anhydrides) (Heat of-combustion)

AKIMOVA, L.N.; GOLUBOVSKAYA, L.Ye.
-------------
Aninoacyl derivatives of amino acid anhydrides,
Vest.Mosk un.ger.2t
Khim. 18 no.2:49-52 Mr-Ap 163. WA 16:5)
1. Kafedra. organicheskoy khimii Moskovskogo
universiteta.
(Amino acids)

AKIMOVA., A.A.; AKIMOVA, L.N.
Behavior of some dipeptides in prolorgoA thermal
extraction with
organic solvents. Vest. Mosk. un. Sei. 2: Xhim. 18
no.5:62-
64 S-0 163. (MIRA 16:11)
1. Kafedra organicheskoy khimii Moskovskogo
universiteta.

'S/076 63/037/001/026/029
B101 Bis6
YB
AUTHORSt Po',,omarev, V,.,. Alekseyeva, T~ A.4 Ai~i-movlk'-L- N-*
TITLEt Heats of combustion of valyl phenyl alanine, phenyl alanyl
anhydride, and glyoyl valyl anhydride
PERIODICAL: Zhurnal fizicheskloy khimii, v. 37, no. 1, 1963, ~27. 228
TEXT-.- Tho heats of combustion were- determ1hed by a
microcalorimeter for
valyl pheryl alanine, phenyl alanyl anhydride, and glycyl valyl
anhydride
that had been chromatographioally-tested for purity. Results: valyl
phenyl alanine, m.p. 236 - 23700i AH - -1816-84 � 0-36; phenyl alanyl
anhydride, m.p. 290 - -2910C, &H 2239 ,01 + 0.221 glyoyl valyl
anhydridel
m.P*..250 - 2510C, 6H . -948-05 1 0.16 kcal/m-ol"e. There is 1 table.
ASSOCIATION: Moskovskiy gosudarstvennyy universitet im'. M. V.
Lomonosova
(Moscow State University imeni M. Vf.- ~omonosov)
2
SUBMITTEDi August 30,1962
Card 1/1

.BOIZISOIIA A.P.; AKIMOVA, L.N.; SAVICII, I.A.
St,idy of the bluret complex of gramicidin C derivatives with
te amino group. Vei3t. Mosk. un. Ser. 2: nim. 20 no,1:33-35
ja-F 165. tMIRA 18-3)
1. Kafedra neorganicheskoy IdAmii r4bskovskogo universiteta.

AKIMOVA, L.N.; VOLKOVA, L.S.
Using double (1v-benzy!c--rbcbBnzoxy'/ protEction for
the synthesis
of optically active peptideq. "lest. Mosk. im.. Ser. 2:
Khim. 20
no.1:65-68 Ja-F '65- (RM IS: 3)
1. Kafedra organicheskoy k-himi MoskovskoFo
universiteta.

L 5
AccEssioN NRi a5aU856
'A -a- - -
blu
"TI7~s Syntbasie of abalate, in1s f awtain aminoatid derivativee
MOM Monow, Vrdytraitirbi' VOA.04:~Aerjya 2. Khimiya., no. 2j, 1965..
91-94
f
TOPIC TAGSi aminoaold, chelate compound
-As -an exteisirn of work reported previously by L, N. Akimova
WE
khimii No 3, 1965) Procedures
for synthesis of methyl I- g
COCCH
O~H
ethyl glycylgirc-inesalJc7late (II)
1-Cord 1/1,

5t,025-65
ACIGEMION NRs -,kP501-1856
2
H
^-~-NCHCO,'4HCHCOOCH,
-OH
N-C.OCHN-
Cti-i
H
HO--'
Hj
Hg

~HN-
%~
CH-FAP~\l
CH,
I
HO-

H C ~Hl

L 55025-65
ACCMION NRi AP5011856
and the Gu(-TV) Ni(V), and Go(VI) complexes of athyl
glycylglycinesalicylate are
T ' -inilt _-J-:1_.l72%M_ not given, M- 196C~, IV- not P-4--
A gi* am hei ing Pdnt I
V- 2600 (chars)3 VJ- 2180. The yields are: 1- 88%3 11- 90%.j III-
90%~ IV-
7- 52%, V-1- 50%. The general formula of the mettl complexes is
CH~N_CHC0_NT"C11,C00CH,
Orig. art. has: 5 for=,las.
AS=WMNj Aloskovskljr titet,, Kited= organichaskoy kh1mii (M6660-~
University.Ljpepartment of Organic Chemistry)
SMUTTED i 26Jun64 ENCLj 00 SUB CODE: OC,,
Aw RU SOV: 005 OTHERx
[ed 3/3
OD7

FRIMIN, S.D.; KLEVXE, v.A.; WLYAYEVA, N.N.;
KIRINDASCFVA, R.Ya.;
SVESHRIKOVA, T.S.; Prinimali uchastiye ~ A& A
M.D.;
FUTORYANSKAYA., M.Ta.
Coridensation of ures, with formaldehydo for the
produotion of
fertilizers with slowly assimilable nitrogen.
Zhur. prikl.
khim. 38 no.5:1091-1097 My 165. (MIRA 18:1-1)

STR'UTINSKIY, V.M.; GROSHEV, L.V.;
Spectra of gamma rays produced in the capture of thermal
neutrons by
heavy nuclei* Part 2. Zhur.ekspA teor.fiz. 38 no.2:598-611 F 160.
(Gamw rays) (Neutrons-Capture) (MIRA 14:5)

88462
4. k B006YB063
AUTHORS: Akimova, M. X.,.Blokhintsev, L. D., Dolinskiy, E. I.
TITLE: Angular Distribution and Polarization of Neutrons
Emitted
in Muon Capture.of Some Light Nuclei
PERIODICAL: Zhurnal eksperimentalinoy-i teorsticheskoy fiziki,
1960,
Vol. 39, No. 6(12), pp., 1806-1617
TEXT: A study of the angular distribution and polarization of
neutrons
emitted from nuclei as a result of the reaotion~k_ + P-M +))
gives
information on the muon-nualoon weak interaction constant.
Formulas for
angular distribution and polarization (Refs. 1-4) have been
obtained in
different approximations, and numerical calculations have been
made for
several concrete cases. The very extensiye calculations
presented here are
based on the theory of universal:Fermi interaction, and have
been made on
the assumption that the interaction of "strippee fermions can
be
described bj V- and A-type four-fermion.coupling. All
relativistic terms
which are of first order in v n/0 (v Z1 -nucleon velocity),
including weak
S/05 60/039/006/054/063
Card 1/8

88462
Angular Distribution and Polarization of,
S/056/60/039/006/054/063
Neutrons Emitted in Muon Capture of Some B006/BO63
Light Nuclei
magnetism and effective pseudoscalar interaction, are taken
into account.
The Hamiltonian H eff describing the muon capture is taken from
Ref. 7,
and from the universal Fermi interaction with conservation of
the vector
current it follows that
9(P ) = 0 - 97 2 g W I +h 4.7 1, 9 0 - �99 9 (P) and
V V A A $
4)- 8g(Pj g(P)- Fermi coupling oonBtantifor P-decay of nucleons;
A V
anomalous magnetic moments of prolton and neutron in nuclear
magnatons; g(P)- Gamow-Teller coupling constant for O-decay of
nucleons.
A
These assumptions and results of a previous paper (Ref. 3) are
used to
derive formulas for the emission probability of neutrons with
given
kinetic energy from a nucleus, for the angular distribution and
the
polarization for the case of direct neutron emission:
Card 2/8

88462
Angular Distribution and Polarization of S/05 60/039/006/054/063
Neutrons'Emitted in Muon Ca-pture of Some Mo6yn63
Lig4t-Huclei
dW (Eiv, 0) G (102W0 (E-Y) II (EA + PIX, (Ev) cos 01 dENdQvl4,T, (4)
I (Ev) (I + UP) *1 2 [1 + 2X~t - %2 (x - 1)],r, (EIV)+
r
+ 1210 + X2 (x I)' + I I T2 (Ev).
K, (Ev) ((-.1 + W) Po (Ev) + 2 f- I + 2,%ji +
~2 X2 (X 1)2
(x (Ev) T, (Eiv) + 12 1 P2 (Ev) T2 (Ev)), (6)
rAe
WIgA
q (Eiv, 0) 1 + Pal (E,v) cos 0, (7)
ct, (EA,) 1