nearest
taken
diagonal
shown
AA
photograph
appropriate
patterson
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treated
bragg
506
IO
fiitered
even
1975
thermalparameterswith
272
final
cromer
294
describing
subsequent
knowledge
SFLS
ramaseshan
432
square
drasekhar
112
position
tribution
262
170
table
359
overlapping
wa
set
PHENYLAZOANILINE
white
could
788
referred
research
425
SUP
7717
peak
642
existence
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474
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absence
character
CH
217
158
infinite
higher
132
symbolic
preliminary
meerten
165
55o
bond
four
spherically
344
crystal
209
individual
670
lographically
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patter
expected
near
calculation
intensitie
105
monoclinic
compatible
bangalore
bare
orange
author
009
ruple
139
129
124
1974
understanding
identified
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presented
description
counterpart
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parameter
original
sec
916
KRIGBAUM
suggested
published
possible
asymmetric
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length
vo
vani
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under
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earlier
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determined
union
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263
group
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crystallographic
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reliable
2813
supplementary
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603
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273
data
131
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ally
376
148
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KALYANI
371
generated
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749
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345
1071
nitrogen
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averaged
method
258
material
141
carbon
detailed
248
weissenberg
798
forming
relevant
phase
procedure
part
weighting
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758
236
MEERTENS
correlation
234
recorded
structural
hereinafter
193
germain
inversion
woolfson
solved
atom
177
increasing
least
introduction
1977
fixed
received
ABER
next
519
almost
110
value
HOEKSTRA
science
mesogenic
227
264
2817
arrangement
function
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respect
non
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vector
ordered
rapidly
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oriented
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385
valency
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214
studie
731
corrected
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328
perpendicular
608
another
view
deposited
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METHOXYBENZYLIDENE
herring
none
470
methoxybenzylidene
156
disorder
fig
vijayan
196
crystallographically
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give
executive
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lie
226
derived
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different
examination
244
discrete
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452
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attempted
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237
IVV
100
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proved
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photographically
171
carried
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441
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907
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126
reliability
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513
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215
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103
separation
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infinitely
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384
temperature
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conference
mentioned
261
321
acta
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subsequently
observed
282
aromatic
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phenyl
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azoxybenzoate
lay
134
above
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A27
153
thank
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536
2237
arising
marked
116
contact
301
plane
phenylazoaniline
chester
calculated
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B31
liquid
interest
poor
137
off
323
212
symmetry
574
P2
TAGA
line
108
result
solution
360
text
CHI
353
ethyl
geometrically
per
computed
257
indicated
parenthese
program
substance
all
british
atomic
1028
198
lorentz
total
flotation
factor
anisotropic
including
704
nematogenic
azo
CROMER
1976
diffuse
multiple
315
recently
smectogenic
560006
317
relative
2240
987
height
284
hoekstra
VANI
I8
pack
azotoluene
they
117
perpen
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main
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conventional
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B33
2236
WOOLFSON
model
national
krigbaum
addition
145
772
509
abnormally
560017
highly
slow
map
measured
study
cule
152
about
CU'
108o
together
VIJAYAN
436
scatter
changing
normal
58o
extra
161
109
observable
random
mclecule
25gcm
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independently
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revealed
spond
chemical
polarization
MAIN
suppl
initial
cryst
consideration
inclined
rest
propertie
mesophase
displaced
feature
corresponding
679
quad
cedure
647
second
scheme
october
reported
fall
174
herringbone
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work
302
professor
pro
three
copie
reference
coordinate
electron
two
each
298
wish
technique
screw
203
it
weight
885
268
829
121
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limit
238
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double
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allowed
laboratory
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refined
146
356
chan
january
methoxy
cupancy
will
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optically
average
389
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crystallography
refiexion
160
exactly
586
bricated
107
ratio
221
then
ring
381
absorption
direct
quadruple
hkl
involving
feasible
formula
thermal
GERMAIN
due
dimensional
independent
curred
reddy
quality
extreme
138
elongated
intensity
occupancy
similar
C6H'
333
described
19o
182
167
854
spot
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analysi
250
solve
2239
between
convenient
space
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276
parallel
mole
though
434
axi
disordered
les
trial
1966b
939
publication
pattern
598
determination
240
england
needle
recalculated
neighbour
using
single
dimension
orthogonal
faded
ing
appeared
clearly
written
within
obtained
IJW
led
516
proceeding
455
level
axe
diffraction
superposing
occurring
triple
1971
orientation
slightly
219
experimental
equal
sider
II
331
struc
them
originally
220
azobenzene
used
considerable
when
translation
418
fashion
friar
hence
aeronautical
further
sign
phenylazoani
institute
adjacent
rotational
567
286
YJ7
ference
816
ion
featuresofthe
conspicuously
BROWN
found
275
glide
2238
lending
crystalline
nearly
low
through
26o
held
clear
numbering
inclination
finalfractional
bfo
610
try
surrounded
245
antiparallel
1965
see
368
ray
either
CZOHI70NJ
correct
paucity
104
maximum
agreed
list
out
modified
201
coloured
consist
NCGH
side
UA
reciprocal
short
I9
169
fourier
extending
1966a
contribution
172
highest
along
not
brown
po
277
division
methoxybenzylidine
reduced
pair
before
evaporation
high
structure