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解方程 (1)3/（x-2)=5/X 3x=5x-10 x=5 (2)1-1/(x-5)=x/(x+5 ) x2-25-x-5=x2-5x 4x=30 x=7.5 计算 (3)(x-2/(x^2-1))+x+1/x^2+2x+1
1-1/(x+1)=2/(x+1)(x-1) 两边乘(x+1)(x-1) x2-1-x+1=2 x2-x-2=0 (x-2)(x+1)=0 x=2,x=-1 经检验，x=-1时公分母(x+1)(x-1)=0 舍去 所以x=2
1/x-1-1/x+1-2/x^2+1-4/x^4+1-8/x^8+1.. =(x+1-x+1)/(x2-1）-2/（x2+1)-4/(x?+1)-8/(x^8+1)... =(2x2+2-2x2+2)/(x?-1)-4/(x?+1)-8/(x^8+1) =(4x?+4-4x?+4)/(x^8-1)-8/(x^8+1) =(8x^8+8-8x^8+...
(1-1/x)÷(x2-2x+1)/(x2-1) =(x-1)/x×(x+1)(x-1)/(x-1)2 =(x+1)/x x=2 原式 =3/2 如果您认可我的回答，请点击“采纳为满意答案”,祝学习进步！
宁静淡泊人生
(2+1/x-1-1/x+1)/(x+x/x^2-1) =(2(x-1)(x+1)+(x+1)-(x-1))/(x-1)(x+1) /(x(x^2-1+1)/(x^2-1)) =(2x^2-2+x+1-x+1)/(x-1)(x+1) *(x^2-1)/x^3 =(2x^2)/(x^2-1) *(x^2-1)/x^3 =2/x
(1-1/x+1)除以x/x^2-1 =(x/(x+1))/(x/(x+1)(x-1))=x-1 x/x-2-3/x+2=1 x(x+2)-3(x-2)=(x+2)(x-2) x^2+4x-3x+6=x^2-4 x=-10
化简[1-1/(1-a)](1/a^2-1);(2a/b)^2-2/b/(b/2a);计算x(2-1/x)+x/(x^2-2x)*(x^2-4)……急急急！！！
x(1-1/7) = 2*(80-x-20) 6x/7=120-2x 6x/7+2x=120 20x/7=120 x=120*7/20 x=42
解：1-1/5(x-10-2x/3)=x/2-1/3(3x-3-6x/2) 30－6[x-﹙10-2x﹚/3]＝15x－10[3x-﹙3-6x﹚/2] 30－6x＋2﹙10-2x﹚＝15x－30x＋5﹙3-6x﹚ 30－6x＋20－4x＝15x－30x＋15－30x －6x－4x－15x＋30x＋30x＝﹣30－20＋15 35x＝﹣35 x＝﹣1
(x^2-1)(1/1+x-1/x-1-1) =(x-1)(x+1)(1/1+x-1/x-1-1) =(x-1)-(x+1)-(x-1)(x+1) =-2-（x平方-1） =-x平方-1百度拇指医生
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3,3,6,6-Tetra-methyl-9-[6-(3,3,6,6-tetra-methyl-1,8-dioxo-2,3,4,5,6,7,8,9-octa-hydro-1H-xanthen-9-yl)pyridin-2-yl]-2,3,4,5,6,7,8,9-octa-hydro-1H-xanthene-1,8-dione.
MedLine Citation:
PubMed-not-MEDLINE
Abstract/OtherAbstract:
In the title mol-ecule, C(39)H(45)NO(6), the two tetra-methyl-octa-hydroxanthen-1,8-dione substituents are arranged approximately parallel to each other and approximately perpendicular to the plane of the pyridine ring. The six-membered xanthene rings adopt flattened boat conformations with the O and methine C atoms deviating from the plane of the other four atoms.
Antar A A Shaaban Kamel M Mirze A A Atash V G Seik Weng Ng
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Acta crystallographica. Section E, Structure reports online
ISO Abbreviation:
Acta Crystallogr Sect E Struct Rep Online
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From MEDLINE(R)/PubMed(R), a database of the U.S. National Library of Medicine
Journal Information
Journal ID (nlm-ta): Acta Crystallogr Sect E Struct Rep Online
Journal ID (publisher-id): Acta Cryst. E
Publisher: International Union of Crystallography
Article Information
A full version of this article is available from Crystallography Journals Online.(C) Abdelhamid et al. 2011
open-access:
Received Day: 21 Month: 2 Year: 2011
Accepted Day: 25 Month: 2 Year: 2011
collection publication date: Day: 01 Month: 4 Year: 2011
Electronic publication date: Day: 05 Month: 3 Year: 2011
pmc-release publication date: Day: 05 Month: 3 Year: 2011
Volume: 67 Issue: Pt 4
First Page: o785 Last Page: o785
ID: 3100053
PubMed Id:
Publisher Id: lh5213
Coden: ACSEBH
Publisher Item Identifier: S7318
3,3,6,6-Tetra-methyl-9-[6-(3,3,6,6-tetra-methyl-1,8-dioxo-2,3,4,5,6,7,8,9-octa-hydro-1H-xanthen-9-yl)pyridin-2-yl]-2,3,4,5,6,7,8,9-octa-hydro-1H-xanthene-1,8-dione
Alternate Title:C39H45NO6
Antar A. Abdelhamid
Shaaban Kamel Mohamed
Mirze A. Allahverdiyev
Atash V. Gurbanov
Seik Weng Ng*
aDepartment of Organic Chemistry, Baku State University, Baku, Azerbaijan
bChemistry & Environmental Science Division, School of Science, Manchester Metropolitan University, UK
cDepartment of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia
Correspondence: Correspondence e-mail: seikweng@um.edu.my
Related literature
For a related structure, see: Mohamed et al. (2011).[Chemical Structure ID: scheme1]
Experimental
Crystal data
Mr = 623.76
Monoclinic,
a = 24.1384 (8) ?
b = 10.0371 (4) ?
c = 14.4408 (5) ?
β = 105.8460 (7)°
Mo Kα radiation
μ = 0.08 mm-1
0.30 × 0.30 × 0.30 mm
Data collection
Bruker APEXII diffractometer
35921 measured reflections
7717 independent reflections
6410 reflections with I & 2σ(I)
Rint = 0.035
Refinement
R[F2 & 2σ(F2)] = 0.041
wR(F2) = 0.111
7717 reflections
415 parameters
H-atom parameters constrained
Δρmax = 0.35 e ?-3
Δρmin = -0.25 e ?-3
Data collection: APEX2 (Bruker, 2005); cell refinement: SAINT (Bruker, 2005); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: X-SEED (Barbour, 2001); software used to prepare material for publication: publCIF (Westrip, 2010).
Supplementary Material
Crystal structure: contains datablocks global, I. DOI: 10./lh5213sup1.cif
Structure factors: contains datablocks I. DOI: 10./lh5213Isup2.hkl
Additional supplementary materials:
crystall 3D checkCIF report
fnu1Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: LH5213).
We thank Manchester Metropolitan University, Baku State University and the University of Malaya for supporting this study.
supplementary crystallographic
information
Experimental
A mixture of 1,2-ethanediammonium chloride (0.01 mol) and
2,6-pyridinedicarbaldehyde (0.01 mol) in aqueous ethanol (1:1) was heated for
30 minutes. To the mixture was added dimedone (0.04 mol). The mixture was
heated for another 5 fhours. The solvent was evaporated to yield a pale yellow
compound. This was recrystallized from ethanol in 60% m.p. 473 K.
Refinement
Carbon-bound H-atoms were placed in calculated positions [C–H 0.95 to 0.99 ?;
U(H) 1.2 to 1.5U(C)] and were included in the refinement in the
riding model approximation.
Crystal data
Data collection
Refinement
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (?2)
Atomic displacement parameters (?2)
Geometric parameters (?, °)
References
Barbour, L. J. (2001). J. Supramol. Chem.1, 189–191.
Bruker (2005). APEX2 and SAINT Bruker AXS Inc., Madison, Wisconsin, USA.
Mohamed, S. K., Abdelhamid, A. A., Khalilov, A. N., Gurbanov, A. V. & Ng, S. W. (2011). Acta Cryst. E67, o850–o851.
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122.
Westrip, S. P. (2010). J. Appl. Cryst.43, 920–925.
[Figure ID: Fap1]
Thermal ellipsoid plot (Barbour, 2001) of C39H45NO6 at the 70% hydrogen atoms are drawn as spheres of arbitrary radius.
[Figure ID: Fap2]
View of the molecule along the pyridyl plane. The pyridyl atoms are shown as 70% thermal ellipsoids in their van der Waals surfaces whereas the other atoms are shown in the ball-and-stick style.
[TableWrap ID: d1e135]
F(000) = 1336
Mr = 623.76
Dx = 1.231 Mg m-3
Monoclinic, P21/c
Mo Kα radiation, λ = 0.71073 ?
Hall symbol:
Cell parameters from 9997 reflections
a = 24.1384 (8) ?
θ = 2.2–28.3°
b = 10.0371 (4) ?
u = 0.08 mm-1
c = 14.4408 (5) ?
β = 105.8460 (7)°
Prism, yellow
0.30 × 0.30 × 0.30 mm
[TableWrap ID: d1e262]
Bruker APEXII diffractometer
6410 reflections with I & 2σ(I)
Radiation source: fine-focus sealed tube
Rint = 0.035
θmax = 27.5°, θmin = 0.9°
φ and ω scans
h = -31→31
35921 measured reflections
k = -13→13
7717 independent reflections
l = -18→18
[TableWrap ID: d1e360]
Refinement on F2
Primary atom site location: structure-invariant direct methods
Least-squares matrix: full
Secondary atom site location: difference Fourier map
R[F2 & 2σ(F2)] = 0.041
Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.111
H-atom parameters constrained
w = 1/[σ2(Fo2) + (0.0516P)2 + 1.4985P]
where P = (Fo2 + 2Fc2)/3
7717 reflections
(Δ/σ)max = 0.001
415 parameters
Δρmax = 0.35 e ?-3
0 restraints
Δρmin = -0.25 e ?-3
[TableWrap ID: d1e519]
0.25761 (4)
0.57513 (8)
0.57197 (6)
0.01520 (18)
0.14471 (4)
0.79864 (10)
0.29720 (7)
0.0240 (2)
0.36827 (4)
0.79429 (9)
0.39499 (7)
0.0219 (2)
0.24055 (4)
0.16338 (10)
0.42959 (6)
0.0194 (2)
0.35334 (4)
0.23059 (10)
0.21320 (7)
0.0235 (2)
0.12820 (4)
0.24399 (11)
0.11215 (7)
0.0283 (2)
0.24746 (4)
0.48227 (10)
0.31079 (7)
0.0153 (2)
0.25467 (5)
0.61420 (12)
0.30329 (8)
0.0139 (2)
0.26132 (5)
0.67429 (13)
0.22082 (9)
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0.25984 (5)
0.59557 (13)
0.14138 (9)
0.0185 (3)
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0.46041 (13)
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0.24614 (5)
0.40734 (12)
0.23306 (8)
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0.25609 (5)
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0.39089 (8)
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0.30987 (5)
0.67488 (12)
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0.72160 (12)
0.46172 (9)
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[TableWrap ID: d1e1657]
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0.0006 (5)
0.0109 (6)
0.0036 (6)
0.0227 (6)
0.0204 (6)
0.0218 (6)
0.0016 (5)
0.0083 (5)
-0.0011 (5)
0.0208 (6)
0.0152 (6)
0.0104 (5)
0.0007 (5)
0.0057 (5)
-0.0006 (4)
0.0193 (6)
0.0141 (6)
0.0151 (6)
0.0009 (5)
0.0065 (5)
-0.0006 (4)
0.0239 (6)
0.0132 (6)
0.0175 (6)
0.0009 (5)
0.0095 (5)
-0.0014 (5)
0.0200 (6)
0.0179 (6)
0.0207 (6)
0.0030 (5)
0.0109 (5)
0.0007 (5)
0.0176 (6)
0.0203 (6)
0.0183 (6)
0.0025 (5)
0.0066 (5)
0.0006 (5)
0.0187 (6)
0.0239 (6)
0.0148 (6)
0.0021 (5)
0.0063 (5)
0.0036 (5)
0.0173 (6)
0.0166 (6)
0.0166 (6)
0.0004 (5)
0.0074 (5)
0.0000 (5)
0.0185 (6)
0.0341 (8)
0.0235 (7)
0.0037 (6)
0.0061 (5)
0.0046 (6)
0.0233 (7)
0.0233 (7)
0.0292 (7)
-0.0004 (5)
0.0072 (6)
-0.0052 (6)
0.0195 (6)
0.0140 (6)
0.0146 (6)
0.0000 (5)
0.0051 (5)
-0.0011 (4)
0.0235 (7)
0.0195 (6)
0.0147 (6)
-0.0002 (5)
0.0039 (5)
-0.0021 (5)
0.0201 (6)
0.0320 (7)
0.0173 (6)
-0.0059 (6)
0.0022 (5)
-0.0038 (5)
0.0186 (6)
0.0196 (6)
0.0174 (6)
-0.0009 (5)
0.0046 (5)
-0.0008 (5)
0.0202 (6)
0.0197 (6)
0.0151 (6)
-0.0002 (5)
0.0065 (5)
0.0024 (5)
0.0172 (6)
0.0152 (6)
0.0149 (6)
0.0007 (5)
0.0035 (5)
-0.0010 (5)
0.0201 (7)
0.0301 (7)
0.0262 (7)
-0.0035 (6)
0.0066 (5)
0.0000 (6)
0.0266 (7)
0.0212 (7)
0.0311 (8)
0.0034 (5)
0.0102 (6)
0.0001 (6)
[TableWrap ID: d1e2473]
1.3757 (14)
1.4926 (17)
1.3800 (14)
1.2242 (16)
1.2242 (15)
1.3732 (15)
1.3761 (15)
1.2220 (15)
1.2200 (16)
1.3438 (16)
1.3443 (15)
1.5060 (17)
1.3829 (17)
1.5082 (17)
1.5264 (16)
1.3853 (18)
1.3393 (17)
1.4688 (17)
1.3771 (18)
1.5157 (18)
1.5335 (17)
1.3865 (16)
1.5270 (17)
1.5261 (18)
1.5051 (17)
1.5296 (19)
1.5133 (16)
1.5325 (17)
1.4884 (17)
1.3393 (17)
1.4696 (17)
1.5103 (17)
1.5338 (18)
1.5321 (19)
1.5336 (18)
1.5387 (17)
1.3363 (17)
1.4958 (17)
1.4687 (17)
1.5129 (18)
1.5301 (18)
1.5293 (18)
1.5292 (18)
1.5341 (18)
1.4903 (17)
1.3368 (17)
1.4719 (17)
1.5111 (18)
1.5328 (18)
1.5269 (17)
1.5332 (18)
1.5403 (17)
C12—O1—C20
118.01 (9)
C18—C21—H21C
C29—O4—C37
117.95 (9)
H21A—C21—H21C
C1—N1—C5
117.26 (10)
H21B—C21—H21C
N1—C1—C2
123.18 (11)
C18—C22—H22A
N1—C1—C6
117.84 (10)
C18—C22—H22B
C2—C1—C6
118.97 (11)
H22A—C22—H22B
C1—C2—C3
118.79 (12)
C18—C22—H22C
C1—C2—H2
H22A—C22—H22C
C3—C2—H2
H22B—C22—H22C
C4—C3—C2
118.78 (11)
C32—C23—C24
108.91 (10)
C4—C3—H3
C32—C23—C5
113.40 (10)
C2—C3—H3
C24—C23—C5
109.91 (10)
C3—C4—C5
119.01 (11)
C32—C23—H23
C3—C4—H4
C24—C23—H23
C5—C4—H4
C5—C23—H23
N1—C5—C4
122.97 (11)
C29—C24—C25
118.76 (11)
N1—C5—C23
118.10 (10)
C29—C24—C23
121.54 (11)
C4—C5—C23
118.87 (11)
C25—C24—C23
119.66 (10)
C15—C6—C7
109.28 (10)
O5—C25—C24
121.22 (12)
C15—C6—C1
112.32 (10)
O5—C25—C26
121.50 (11)
C7—C6—C1
111.35 (10)
C24—C25—C26
117.23 (10)
C15—C6—H6
C25—C26—C27
112.66 (10)
C7—C6—H6
C25—C26—H26A
C1—C6—H6
C27—C26—H26A
C12—C7—C8
118.80 (11)
C25—C26—H26B
C12—C7—C6
122.23 (11)
C27—C26—H26B
C8—C7—C6
118.95 (10)
H26A—C26—H26B
O3—C8—C7
120.99 (11)
C30—C27—C31
108.98 (11)
O3—C8—C9
121.47 (11)
C30—C27—C28
108.65 (11)
C7—C8—C9
117.52 (10)
C31—C27—C28
110.25 (11)
C8—C9—C10
114.25 (10)
C30—C27—C26
110.53 (11)
C8—C9—H9A
C31—C27—C26
110.34 (11)
C10—C9—H9A
C28—C27—C26
108.06 (10)
C8—C9—H9B
C29—C28—C27
112.24 (10)
C10—C9—H9B
C29—C28—H28A
H9A—C9—H9B
C27—C28—H28A
C14—C10—C13
109.05 (11)
C29—C28—H28B
C14—C10—C9
109.82 (11)
C27—C28—H28B
C13—C10—C9
109.49 (11)
H28A—C28—H28B
C14—C10—C11
110.21 (11)
C24—C29—O4
122.55 (11)
C13—C10—C11
108.83 (11)
C24—C29—C28
126.06 (11)
C9—C10—C11
109.42 (10)
O4—C29—C28
111.39 (10)
C12—C11—C10
113.69 (10)
C27—C30—H30A
C12—C11—H11A
C27—C30—H30B
C10—C11—H11A
H30A—C30—H30B
C12—C11—H11B
C27—C30—H30C
C10—C11—H11B
H30A—C30—H30C
H11A—C11—H11B
H30B—C30—H30C
C7—C12—O1
122.73 (11)
C27—C31—H31A
C7—C12—C11
126.18 (11)
C27—C31—H31B
O1—C12—C11
111.07 (10)
H31A—C31—H31B
C10—C13—H13A
C27—C31—H31C
C10—C13—H13B
H31A—C31—H31C
H13A—C13—H13B
H31B—C31—H31C
C10—C13—H13C
C37—C32—C33
118.51 (11)
H13A—C13—H13C
C37—C32—C23
121.95 (11)
H13B—C13—H13C
C33—C32—C23
119.49 (11)
C10—C14—H14A
O6—C33—C32
121.28 (12)
C10—C14—H14B
O6—C33—C34
121.44 (12)
H14A—C14—H14B
C32—C33—C34
117.21 (11)
C10—C14—H14C
C33—C34—C35
114.32 (11)
H14A—C14—H14C
C33—C34—H34A
H14B—C14—H14C
C35—C34—H34A
C20—C15—C16
118.88 (11)
C33—C34—H34B
C20—C15—C6
122.60 (11)
C35—C34—H34B
C16—C15—C6
118.50 (11)
H34A—C34—H34B
O2—C16—C15
120.94 (12)
C38—C35—C39
109.44 (11)
O2—C16—C17
121.57 (11)
C38—C35—C34
109.89 (11)
C15—C16—C17
117.48 (11)
C39—C35—C34
110.57 (11)
C16—C17—C18
113.85 (10)
C38—C35—C36
109.23 (11)
C16—C17—H17A
C39—C35—C36
109.89 (11)
C18—C17—H17A
C34—C35—C36
107.79 (10)
C16—C17—H17B
C37—C36—C35
112.36 (10)
C18—C17—H17B
C37—C36—H36A
H17A—C17—H17B
C35—C36—H36A
C21—C18—C17
109.83 (11)
C37—C36—H36B
C21—C18—C22
108.80 (11)
C35—C36—H36B
C17—C18—C22
109.51 (11)
H36A—C36—H36B
C21—C18—C19
108.62 (10)
C32—C37—O4
122.38 (11)
C17—C18—C19
108.78 (10)
C32—C37—C36
126.52 (11)
C22—C18—C19
111.30 (10)
O4—C37—C36
111.08 (10)
C20—C19—C18
112.98 (10)
C35—C38—H38A
C20—C19—H19A
C35—C38—H38B
C18—C19—H19A
H38A—C38—H38B
C20—C19—H19B
C35—C38—H38C
C18—C19—H19B
H38A—C38—H38C
H19A—C19—H19B
H38B—C38—H38C
C15—C20—O1
122.60 (11)
C35—C39—H39A
C15—C20—C19
126.13 (11)
C35—C39—H39B
O1—C20—C19
111.25 (10)
H39A—C39—H39B
C18—C21—H21A
C35—C39—H39C
C18—C21—H21B
H39A—C39—H39C
H21A—C21—H21B
H39B—C39—H39C
C5—N1—C1—C2
-0.78 (18)
C6—C15—C20—C19
179.61 (11)
C5—N1—C1—C6
179.85 (10)
C12—O1—C20—C15
11.41 (16)
N1—C1—C2—C3
C12—O1—C20—C19
-166.90 (10)
C6—C1—C2—C3
-179.82 (11)
C18—C19—C20—C15
-20.41 (18)
C1—C2—C3—C4
C18—C19—C20—O1
157.83 (10)
C2—C3—C4—C5
-1.12 (18)
N1—C5—C23—C32
58.96 (14)
C1—N1—C5—C4
-0.24 (17)
C4—C5—C23—C32
-123.78 (12)
C1—N1—C5—C23
176.90 (10)
N1—C5—C23—C24
-63.20 (14)
C3—C4—C5—N1
C4—C5—C23—C24
114.06 (12)
C3—C4—C5—C23
-175.93 (11)
C32—C23—C24—C29
-20.88 (16)
N1—C1—C6—C15
-54.14 (14)
C5—C23—C24—C29
103.91 (13)
C2—C1—C6—C15
126.46 (12)
C32—C23—C24—C25
161.34 (10)
N1—C1—C6—C7
68.80 (14)
C5—C23—C24—C25
-73.87 (13)
C2—C1—C6—C7
-110.60 (12)
C29—C24—C25—O5
-177.42 (12)
C15—C6—C7—C12
14.18 (16)
C23—C24—C25—O5
C1—C6—C7—C12
-110.48 (13)
C29—C24—C25—C26
C15—C6—C7—C8
-164.21 (10)
C23—C24—C25—C26
-177.15 (11)
C1—C6—C7—C8
71.13 (13)
O5—C25—C26—C27
146.24 (12)
C12—C7—C8—O3
-169.42 (12)
C24—C25—C26—C27
-36.19 (15)
C6—C7—C8—O3
C25—C26—C27—C30
175.29 (11)
C12—C7—C8—C9
11.97 (17)
C25—C26—C27—C31
-64.09 (14)
C6—C7—C8—C9
-169.59 (10)
C25—C26—C27—C28
56.52 (14)
O3—C8—C9—C10
143.94 (12)
C30—C27—C28—C29
-167.43 (11)
C7—C8—C9—C10
-37.46 (15)
C31—C27—C28—C29
73.20 (14)
C8—C9—C10—C14
-70.02 (14)
C26—C27—C28—C29
-47.46 (14)
C8—C9—C10—C13
170.28 (11)
C25—C24—C29—O4
-175.58 (11)
C8—C9—C10—C11
51.08 (14)
C23—C24—C29—O4
C14—C10—C11—C12
79.67 (13)
C25—C24—C29—C28
C13—C10—C11—C12
-160.79 (11)
C23—C24—C29—C28
-174.13 (12)
C9—C10—C11—C12
-41.18 (14)
C37—O4—C29—C24
11.94 (18)
C8—C7—C12—O1
175.34 (10)
C37—O4—C29—C28
-167.41 (10)
C6—C7—C12—O1
-3.05 (18)
C27—C28—C29—C24
19.21 (18)
C8—C7—C12—C11
-2.85 (19)
C27—C28—C29—O4
-161.47 (10)
C6—C7—C12—C11
178.76 (11)
C24—C23—C32—C37
19.29 (16)
C20—O1—C12—C7
-10.61 (16)
C5—C23—C32—C37
-103.42 (14)
C20—O1—C12—C11
167.82 (10)
C24—C23—C32—C33
-158.13 (11)
C10—C11—C12—C7
18.90 (18)
C5—C23—C32—C33
79.16 (14)
C10—C11—C12—O1
-159.47 (10)
C37—C32—C33—O6
-179.69 (13)
C7—C6—C15—C20
-13.46 (16)
C23—C32—C33—O6
-2.18 (19)
C1—C6—C15—C20
110.63 (13)
C37—C32—C33—C34
-2.84 (18)
C7—C6—C15—C16
165.04 (10)
C23—C32—C33—C34
174.67 (11)
C1—C6—C15—C16
-70.86 (13)
O6—C33—C34—C35
-149.70 (13)
C20—C15—C16—O2
172.25 (12)
C32—C33—C34—C35
33.45 (17)
C6—C15—C16—O2
-6.31 (17)
C33—C34—C35—C38
-173.37 (12)
C20—C15—C16—C17
-8.86 (17)
C33—C34—C35—C39
65.70 (15)
C6—C15—C16—C17
172.58 (10)
C33—C34—C35—C36
-54.43 (15)
O2—C16—C17—C18
-144.91 (12)
C38—C35—C36—C37
166.01 (11)
C15—C16—C17—C18
36.21 (15)
C39—C35—C36—C37
-73.91 (14)
C16—C17—C18—C21
-171.76 (11)
C34—C35—C36—C37
46.65 (14)
C16—C17—C18—C22
68.82 (13)
C33—C32—C37—O4
174.15 (11)
C16—C17—C18—C19
-53.01 (14)
C23—C32—C37—O4
-3.29 (19)
C21—C18—C19—C20
163.90 (11)
C33—C32—C37—C36
-3.85 (19)
C17—C18—C19—C20
44.39 (14)
C23—C32—C37—C36
178.71 (11)
C22—C18—C19—C20
-76.35 (13)
C29—O4—C37—C32
-13.67 (17)
C16—C15—C20—O1
-176.94 (10)
C29—O4—C37—C36
164.61 (10)
C6—C15—C20—O1
C35—C36—C37—C32
-19.89 (18)
C16—C15—C20—C19
C35—C36—C37—O4
161.92 (10)
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