Literature DB >> 25552965

Definitive crystal structure of 1,1'-bis-[1,2-dicarba-closo-dodeca-borane(11)].

Wing Y Man1, Georgina M Rosair1, Alan J Welch1.   

Abstract

In the title compound, C4H22B20, the two {1,2-closo-C2B10H11} cages are linked across a centre of inversion with a C-C distance of 1.5339 (11) Å. By careful analysis of the structure, it is established that the non-linking cage C atom is equally disordered over cage vertices 2 and 3.

Entities:  

Keywords:  1,2-dicarba-closo-dodeca­borane(11); cage compounds; carboranes; crystal structure

Year:  2014        PMID: 25552965      PMCID: PMC4257441          DOI: 10.1107/S1600536814023897

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Chemical context

The chemistry of single-cage carboranes is now regarded as a mature subject (Grimes, 2011 ▶) but that of bis­(carboranes), two discrete carborane units connected via a two-centre–two-electron bond, is far from fully developed. For bis­(carboranes) composed of two C2B10 icosa­hedra, there are several possible isomers of which 1,1′-bis­[1,2-dicarba-closo-dodeca­borane(11)] (Dupont & Hawthorne, 1964 ▶) is the best known. Aspects of the chemistry of this species have been partially explored (Hawthorne & Owen, 1971 ▶; Yanovsky et al., 1979 ▶; Harwell et al., 1996 ▶, 1997 ▶; Herzog et al., 1999 ▶; Ellis et al., 2010a ▶,b ▶) but there is still considerable scope for further development. The two structural studies of 1,1′-bis­[1,2-dicarba-closo-dodeca­borane(11)] so far reported for which atomic coordin­ates are available (Hall et al., 1965 ▶; Ren & Xie, 2008 ▶) agree that the overall mol­ecular structure is that of two 1,2-dicarba-closo-dodeca­borane(11) units linked via a C1—C1A bond across a centre of inversion. However they differ in their inter­pretation of the position of the non-linking carbon atom, C2 (and, by symmetry, C2A). In the earlier study, Hall et al. considered two models, one (Case I) in which C2 was disordered over two adjacent cage vertices and another (Case II) in which it was disordered over all five vertices to which C1 is connected, expressing a slight preference for the former model based on R factors, with supplementary evidence coming from inspection of temperature factors and the lengths of cage connectivities. In their later study, Ren & Xie considered only an ordered model, with C2 occupying one of the two C/B disordered sites in Case I of Hall et al., but no justification for this model was given. The two crystals used by Hall et al. and by Ren & Xie are isomorphous, and both data sets were collected at room temperature. We have recently described two new methods, which distinguish CH from BH vertices in carboranes and heterocarboranes, the Vertex-to-Centroid Distance (VCD) method (McAnaw et al., 2013 ▶) and the BoronHydrogen Distance (BHD) method (McAnaw et al., 2014 ▶). In the present communication, we apply these methods to a precise, low-temperature data set to unambiguously describe the crystal structure of the title compound, 1,1′-bis­[1,2-dicarba-closo-dodeca­borane(11)].

Structural commentary

Mol­ecules of 1,1′-bis­[1,2-dicarba-closo-dodeca­borane(11)] are composed of two {1,2-closo-C2B10H11} cages (the contents of one asymmetric fraction of the unit cell), linked across a crystallographic inversion centre by the C1–C1A bond [1.5339 (11) Å; symmetry code: (A) −x, −y + 2, −z + 2] (Fig. 1 ▶). The two cages are essentially co-linear, with B12⋯C1—C1A = 175.14 (5)°.
Figure 1

Perspective view of the title compound, with displacement ellipsoids drawn at the 50% probability level. The label suffix ‘A’ refers to the symmetry operation (−x, −y + 2, −z + 2).

The crystals used in this determination are also isomorphous with those studied by Hall et al. (1965 ▶) and by Ren & Xie (2008 ▶), so comment on the positioning of the non-linking cage C atom in all three determinations is warranted. Using the Vertex-to-Centroid Distance (VCD) method (McAnaw et al., 2013 ▶) to analyse our Prostructure (only the linking atom C1 identified as carbon with all other cage atoms described as boron and with H atoms allowed positional refinement), we conclude that the second cage C atom is statistically disordered over vertices 2 and 3 (Table 1 ▶). On assigning these positions as (essentially) 0.5C+0.5B and completing the refinement we note that all vertex–centroid distances barely change, confirming our contention (McAnaw et al., 2013 ▶) that the conclusions from the VCD method are essentially independent of whether vertices have been refined as C or B and thus allowing the method to be applied to literature structures even if an incorrect C/B assignment has been made. Application of the VCD method to the structure of Hall et al. confirms that their partially disordered Case I model was correct, whilst application to the structure of Ren & Xie (which had the second C atom exclusively at vertex 3) shows that their model is incorrect. BoronHydrogen Distance (BHD) analysis (McAnaw et al., 2014 ▶) of our structure (Table 2 ▶) also supports the conclusion that the non-linking C is disordered over vertices 2 and 3. The two shortest vertex–H distances in the Prostructure involve vertices 2 and 3, and when these vertices are assigned as (essentially) 0.5C+0.5B, the refined distances to H increase to values between those expected for 100% B and 100% C.
Table 1

Vertex-to-centroid distances () in studies of 1,1-bis[1,2-dicarba-closo-dodecaborane(11)]

VertexHall et al. (1965)Ren Zie (2008)This study (Prostructure)This study (final structure)
11.5890(10)1.590(2)1.5969(8)1.5975(6)
21.6274(13)1.627(2)1.6385(10)1.6384(7)
31.6291(12)1.632(2)1.6420(9)1.6418(7)
41.6893(13)1.700(2)1.7129(9)1.7117(7)
51.6938(14)1.692(2)1.7069(9)1.7054(7)
61.6817(13)1.696(2)1.7145(9)1.7124(7)
71.6904(14)1.694(3)1.7085(9)1.7086(7)
81.6839(15)1.685(3)1.7002(10)1.7002(7)
91.6740(15)1.681(3)1.6920(10)1.6920(7)
101.6717(15)1.672(3)1.6900(10)1.6900(8)
111.6888(14)1.685(3)1.7020(10)1.7019(8)
121.6657(16)1.665(3)1.6779(10)1.6780(8)
Table 2

Vertex-to-H distances () in Prostructure and final structure of 1,1-bis[1,2-dicarba-closo-dodecaborane(11)]

VertexDistance (Prostructure)Distance (final structure)
20.842(12)1.030(9)
30.902(11)1.006(9)
41.066(11)1.083(9)
51.105(11)1.094(8)
61.088(11)1.096(8)
71.110(11)1.089(9)
81.088(11)1.069(9)
91.043(12)1.080(9)
101.164(12)1.108(9)
111.118(11)1.096(9)
121.086(11)1.108(9)
The final structure determined for 1,1′-bis­[1,2-dicarba-closo-dodeca­borane(11)] is the most precise to date. The e.s.d.’s on comparable mol­ecular parameters are ca half the magnitude of those of Hall et al. (which is nevertheless a remarkably good determination given the hardware used to collect data and the limited number of reflections measured) and ca a quarter of the magnitude of those of Ren & Xie. The present determination is the only one to have been carried out at low temperature (100 K). The three C1—B distances span the range 1.7308 (9)–1.7427 (9) Å whilst the two C1—C/B connectivities are 1.6950 (8) and 1.6991 (8) Å. Of the remaining connectivities, C/B—C/B is shortest, 1.7215 (9) Å, C/B—B is inter­mediate, lying in the range 1.7353 (10)–1.7603 (9) Å, and B—B distances are the longest, spanning from 1.7775 (10) to 1.8015 (11) Å. The relative lengths of all of these connectivities are fully consistent with the fact that C has a smaller radius than B, which is the essential basis for the VCD method.

Supra­molecular features

The only H⋯H contact less than 2.40 Å is H3⋯H12B at 2.342 (13) Å [symmetry code: (B) −x + , y + , −z + ]. Given that vertex B is 50% C and that CH units and BH units in carboranes are protonic and hydridic respectively, with the degree of hydridic character increasing with increasing distance from the C atoms, this might represent a weak di­hydrogen bond. The angles at H3 and H12B are 151.1 (7) and 123.2 (6)°, respectively.

Database survey

A search of the Cambridge Structural Database (Groom & Allen, 2014 ▶) for the 1,1′-bis­(1,2-dicarba-closo-dodeca­borane) unit using Conquest (Version 1.16) returns 13 hits. Of these, four are reported to be of the title compound (DOCBOR, DOCBOR01, DOCBOR02 and DOCBOR03). DOCBOR (Hall et al., 1965 ▶) represents an early (room-temperature data, point detector, <2000 reflections collected) yet remarkably precise determination. DOCBOR01 (Swanson et al., 1968 ▶) appears to be a powder diffraction study and certainly no resulting atomic coordinates are deposited. DOCBOR02 (Yang et al., 1995 ▶) is ambiguously recorded in the Database; the actual mol­ecule which is the subject of the crystallographic study (compound 2 in the relevant paper) is [1-(3′-1′,2′-closo-C2B10H11)-2-closo-C2B10H11] with a C1—B3′ inter­cluster bond whereas 1,1′-bis­[1,2-dicarba-closo-dodeca­borane(11)] is [1-(1′-1′,2′-closo-C2B10H11)-2-closo-C2B10H11] with a C1—C1′ inter­cluster bond. Finally, the most recent published determination (DOCBOR03; Ren & Xie, 2008 ▶) involves data collected on a modern CCD-equipped diffractometer although also at room temperature. Of the remaining nine hits revealed by Conquest, one (FASQAR; Herzog et al., 1999 ▶) relates to an octa­methyl derivative of 1,1′-bis­[1,2-dicarba-closo-dodeca­borane(11)] and eight are concerned with species in which the mol­ecule has been deprotonated at the C2 and C2′ positions, with the resulting dianion complexing either a transition metal or a main-group element.

Synthesis and crystallization

The compound was prepared by the CuI-mediated coupling of li­thia­ted ortho-carborane, a method first reported by Yang et al. (1995 ▶) for para-carborane and later used by Ren & Xie (2008 ▶) for the coupling of ortho-carborane. Purity was confirmed by elemental microanalysis, mass spectrometry and NMR spectroscopy, the last by comparison with the data of Yang et al. (1995 ▶). Single crystals for this study were afforded by cooling a solution of the compound in hexane to 243 K.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 3 ▶. The mol­ecule sits on a crystallographic centre of symmetry at the mid-point of the C1—C1A bond. Initially only the linking atom C1 was identified as carbon, with all other cage atoms described as boron and with H atoms allowed positional refinement. This model (the Prostructure) was refined and then analysed by both the VCD (McAnaw et al., 2013 ▶) and the BHD (McAnaw et al., 2014 ▶) methods. Both methods led to the same conclusion regarding the location of the second C atom, which was found to be disordered between positions 2 and 3. These vertices were assigned boron and carbon occupancies of 0.5, treated as tied variables. Refinement was completed with H atoms continuing to be refined positionally and with U iso(H) = 1.2U eq(C,B). At convergence, cage position 2 is [0.503 (9) C + 0.497 (9) B] and cage position 3 [0.497 (9) C + 0.503 (9) B]; effectively positions 2 and 3 are both 50% C + 50% B.
Table 3

Experimental details

Crystal data
Chemical formulaC4H22B20
M r 286.41
Crystal system, space groupMonoclinic, P21/n
Temperature (K)100
a, b, c ()7.0011(5), 9.7667(6), 12.4071(8)
()90.375(3)
V (3)848.35(10)
Z 2
Radiation typeMo K
(mm1)0.05
Crystal size (mm)0.38 0.34 0.32
 
Data collection
DiffractometerBruker APEXII CCD
Absorption correctionMulti-scan (SADABS; Bruker, 2008)
T min, T max 0.706, 0.747
No. of measured, independent and observed [I > 2(I)] reflections22850, 3324, 2787
R int 0.029
(sin /)max (1)0.778
 
Refinement
R[F 2 > 2(F 2)], wR(F 2), S 0.036, 0.106, 1.05
No. of reflections3324
No. of parameters143
H-atom treatmentOnly H-atom coordinates refined
max, min (e 3)0.30, 0.22

Computer programs: SAINT and APEX2 (Bruker, 2009 ▶), SHELXS97 and SHELXL2014 (Sheldrick, 2008 ▶) and OLEX2 (Dolomanov et al., 2009 ▶).

Crystal structure: contains datablock(s) I. DOI: 10.1107/S1600536814023897/pk2536sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536814023897/pk2536Isup2.hkl CCDC reference: 1031659 Additional supporting information: crystallographic information; 3D view; checkCIF report
C4H22B20F(000) = 292
Mr = 286.41Dx = 1.121 Mg m3
Monoclinic, P21/nMo Kα radiation, λ = 0.71073 Å
a = 7.0011 (5) ÅCell parameters from 7872 reflections
b = 9.7667 (6) Åθ = 3.3–33.5°
c = 12.4071 (8) ŵ = 0.05 mm1
β = 90.375 (3)°T = 100 K
V = 848.35 (10) Å3BLOCK, colourless
Z = 20.38 × 0.34 × 0.32 mm
Bruker APEXII CCD diffractometer3324 independent reflections
Radiation source: sealed tube2787 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.029
φ and ω scansθmax = 33.6°, θmin = 2.7°
Absorption correction: multi-scan (SADABS; Bruker, 2008)h = −10→10
Tmin = 0.706, Tmax = 0.747k = −14→15
22850 measured reflectionsl = −19→19
Refinement on F20 restraints
Least-squares matrix: fullHydrogen site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.036Only H-atom coordinates refined
wR(F2) = 0.106w = 1/[σ2(Fo2) + (0.0556P)2 + 0.1013P] where P = (Fo2 + 2Fc2)/3
S = 1.05(Δ/σ)max < 0.001
3324 reflectionsΔρmax = 0.30 e Å3
143 parametersΔρmin = −0.22 e Å3
Experimental. Absorption correction: SADABS-2008/1 (Bruker, 2008) was used for absorption correction. wR2(int) was 0.0508 before and 0.0428 after correction. The Ratio of minimum to maximum transmission is 0.9456. The λ/2 correction factor is 0.0015.
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.
xyzUiso*/UeqOcc. (<1)
C1−0.00588 (8)0.94081 (6)0.95949 (4)0.01437 (11)
B2−0.07903 (9)0.98070 (7)0.83283 (5)0.01927 (14)0.497 (9)
H2−0.1071 (12)1.0828 (10)0.8194 (7)0.023*
B30.15654 (9)0.94099 (7)0.85833 (5)0.01846 (13)0.503 (9)
H30.2474 (12)1.0207 (9)0.8580 (7)0.022*
B40.17020 (10)0.81469 (7)0.95931 (5)0.01763 (13)
H40.2854 (12)0.8236 (9)1.0176 (7)0.021*
B5−0.07164 (10)0.77626 (7)0.99536 (5)0.01763 (13)
H5−0.1033 (12)0.7563 (9)1.0801 (7)0.021*
B6−0.22796 (9)0.88235 (7)0.91629 (5)0.01762 (13)
H6−0.3531 (12)0.9333 (9)0.9506 (7)0.021*
B70.04606 (10)0.87930 (7)0.74140 (5)0.01979 (14)
H70.0862 (12)0.9264 (9)0.6652 (7)0.024*
B80.20135 (10)0.77266 (7)0.82037 (6)0.01995 (14)
H80.3405 (12)0.7451 (10)0.7928 (7)0.024*
B90.05645 (11)0.66684 (7)0.90524 (6)0.02070 (14)
H90.1038 (12)0.5664 (9)0.9302 (7)0.025*
B10−0.19002 (11)0.70885 (7)0.87886 (6)0.02095 (14)
H10−0.3091 (13)0.6353 (10)0.8892 (7)0.025*
B11−0.19577 (10)0.84046 (8)0.77730 (6)0.02052 (14)
H11−0.3151 (12)0.8578 (10)0.7213 (7)0.025*
B12−0.02108 (11)0.70670 (7)0.77061 (6)0.02187 (14)
H12−0.0230 (12)0.6296 (10)0.7051 (7)0.026*
C2−0.07903 (9)0.98070 (7)0.83283 (5)0.01927 (14)0.503 (9)
C30.15654 (9)0.94099 (7)0.85833 (5)0.01846 (13)0.497 (9)
U11U22U33U12U13U23
C10.0157 (2)0.0151 (2)0.0123 (2)−0.00095 (18)0.00111 (17)0.00166 (16)
B20.0196 (3)0.0240 (3)0.0142 (3)−0.0027 (2)0.0005 (2)−0.0006 (2)
B30.0220 (3)0.0187 (3)0.0147 (3)0.0011 (2)0.0012 (2)0.0010 (2)
B40.0191 (3)0.0170 (3)0.0169 (3)0.0020 (2)0.0016 (2)0.0020 (2)
B50.0208 (3)0.0155 (3)0.0166 (3)−0.0018 (2)0.0022 (2)0.0021 (2)
B60.0171 (3)0.0188 (3)0.0169 (3)−0.0023 (2)0.0000 (2)0.0001 (2)
B70.0240 (3)0.0212 (3)0.0141 (3)−0.0009 (2)0.0019 (2)0.0001 (2)
B80.0222 (3)0.0195 (3)0.0181 (3)0.0015 (2)0.0040 (2)−0.0002 (2)
B90.0262 (3)0.0162 (3)0.0198 (3)0.0004 (2)0.0036 (2)0.0007 (2)
B100.0244 (3)0.0183 (3)0.0202 (3)−0.0044 (2)0.0017 (2)−0.0017 (2)
B110.0225 (3)0.0222 (3)0.0168 (3)−0.0026 (2)−0.0017 (2)−0.0013 (2)
B120.0273 (3)0.0198 (3)0.0185 (3)−0.0025 (3)0.0023 (2)−0.0022 (2)
C20.0196 (3)0.0240 (3)0.0142 (3)−0.0027 (2)0.0005 (2)−0.0006 (2)
C30.0220 (3)0.0187 (3)0.0147 (3)0.0011 (2)0.0012 (2)0.0010 (2)
C1—C1i1.5339 (11)B6—H61.096 (8)
C1—B21.6950 (8)B6—B101.7775 (10)
C1—B31.6991 (8)B6—B111.7881 (10)
C1—B41.7427 (9)B6—C21.7596 (9)
C1—B51.7308 (9)B7—H71.089 (9)
C1—B61.7378 (9)B7—B81.7924 (10)
C1—C21.6950 (8)B7—B111.7941 (10)
C1—C31.6991 (8)B7—B121.7877 (10)
B2—H21.030 (9)B7—C21.7457 (9)
B2—B61.7596 (9)B7—C31.7468 (9)
B2—B71.7457 (9)B8—H81.069 (9)
B2—B111.7353 (10)B8—B91.7944 (10)
B2—C31.7215 (9)B8—B121.7912 (11)
B3—H31.006 (9)B8—C31.7392 (10)
B3—B41.7603 (9)B9—H91.080 (9)
B3—B71.7468 (9)B9—B101.8015 (11)
B3—B81.7392 (10)B9—B121.7956 (10)
B3—C21.7215 (9)B10—H101.108 (9)
B4—H41.083 (9)B10—B111.8003 (10)
B4—B51.7937 (10)B10—B121.7956 (10)
B4—B81.7869 (10)B11—H111.096 (9)
B4—B91.7784 (10)B11—B121.7918 (11)
B4—C31.7603 (9)B11—C21.7353 (10)
B5—H51.094 (8)B12—H121.108 (9)
B5—B61.7944 (10)C2—H21.030 (9)
B5—B91.7915 (10)C3—H31.006 (9)
B5—B101.7871 (10)
C1i—C1—B2116.67 (6)C2—B7—B359.07 (4)
C1i—C1—B3116.75 (6)C2—B7—H7117.2 (5)
C1i—C1—B4119.91 (6)C2—B7—B8106.23 (5)
C1i—C1—B5123.00 (5)C2—B7—B1158.69 (4)
C1i—C1—B6119.59 (6)C2—B7—B12105.64 (5)
C1i—C1—C2116.67 (6)C3—B7—H7117.4 (5)
C1i—C1—C3116.75 (6)C3—B7—B858.85 (4)
B2—C1—B4111.76 (4)C3—B7—B11106.28 (5)
B2—C1—B5111.87 (4)C3—B7—B12105.81 (5)
B2—C1—B661.66 (4)B3—B8—B459.88 (4)
B2—C1—C360.96 (4)B3—B8—B759.27 (4)
B3—C1—B461.51 (4)B3—B8—H8119.4 (5)
B3—C1—B5111.80 (4)B3—B8—B9106.37 (5)
B3—C1—B6111.98 (4)B3—B8—B12105.98 (5)
B5—C1—B462.18 (4)B4—B8—B7108.45 (5)
B5—C1—B662.31 (4)B4—B8—H8118.9 (5)
B6—C1—B4113.51 (5)B4—B8—B959.55 (4)
C2—C1—B360.96 (4)B4—B8—B12107.69 (5)
C2—C1—B4111.76 (4)B7—B8—H8121.5 (5)
C2—C1—B5111.87 (4)B7—B8—B9108.19 (5)
C2—C1—B661.66 (4)B9—B8—H8124.3 (5)
C3—C1—B461.51 (4)B12—B8—B759.85 (4)
C3—C1—B5111.80 (4)B12—B8—H8126.2 (5)
C3—C1—B6111.98 (4)B12—B8—B960.10 (4)
C1—B2—H2115.4 (5)C3—B8—B459.88 (4)
C1—B2—B660.37 (4)C3—B8—B759.27 (4)
C1—B2—B7108.80 (5)C3—B8—H8119.4 (5)
C1—B2—B11108.99 (5)C3—B8—B9106.37 (5)
C1—B2—C359.64 (4)C3—B8—B12105.98 (5)
B6—B2—H2120.7 (5)B4—B9—B560.32 (4)
B7—B2—H2122.7 (5)B4—B9—B860.02 (4)
B7—B2—B6111.99 (5)B4—B9—H9119.6 (5)
B11—B2—H2127.7 (5)B4—B9—B10108.04 (5)
B11—B2—B661.54 (4)B4—B9—B12107.87 (5)
B11—B2—B762.04 (4)B5—B9—B8108.05 (5)
C3—B2—H2115.4 (5)B5—B9—H9121.1 (5)
C3—B2—B6109.85 (5)B5—B9—B1059.65 (4)
C3—B2—B760.50 (4)B5—B9—B12107.56 (5)
C3—B2—B11110.08 (5)B8—B9—H9121.2 (5)
C1—B3—H3115.5 (5)B8—B9—B10107.86 (5)
C1—B3—B460.47 (4)B8—B9—B1259.86 (4)
C1—B3—B7108.56 (5)B10—B9—H9123.4 (5)
C1—B3—B8108.78 (5)B12—B9—H9123.6 (5)
C1—B3—C259.40 (3)B12—B9—B1059.89 (4)
B4—B3—H3120.9 (5)B5—B10—B959.89 (4)
B7—B3—H3122.7 (5)B5—B10—H10119.4 (5)
B7—B3—B4111.79 (5)B5—B10—B11108.13 (5)
B8—B3—H3128.0 (5)B5—B10—B12107.76 (5)
B8—B3—B461.40 (4)B6—B10—B560.45 (4)
B8—B3—B761.88 (4)B6—B10—B9108.32 (5)
C2—B3—H3115.5 (5)B6—B10—H10118.3 (5)
C2—B3—B4109.64 (5)B6—B10—B1159.97 (4)
C2—B3—B760.44 (4)B6—B10—B12107.87 (5)
C2—B3—B8109.72 (5)B9—B10—H10123.5 (5)
C1—B4—B358.03 (3)B11—B10—B9107.86 (5)
C1—B4—H4117.8 (5)B11—B10—H10122.0 (5)
C1—B4—B558.58 (4)B12—B10—B959.89 (4)
C1—B4—B8104.74 (4)B12—B10—H10125.3 (5)
C1—B4—B9105.03 (5)B12—B10—B1159.77 (4)
C1—B4—C358.03 (3)B2—B11—B659.90 (4)
B3—B4—H4117.1 (5)B2—B11—B759.26 (4)
B3—B4—B5106.09 (5)B2—B11—B10106.10 (5)
B3—B4—B858.72 (4)B2—B11—H11119.0 (5)
B3—B4—B9106.16 (5)B2—B11—B12105.90 (5)
B5—B4—H4123.4 (5)B6—B11—B7108.43 (5)
B8—B4—H4124.6 (5)B6—B11—B1059.38 (4)
B8—B4—B5108.29 (5)B6—B11—H11118.4 (5)
B9—B4—H4130.3 (5)B6—B11—B12107.57 (5)
B9—B4—B560.20 (4)B7—B11—B10107.93 (5)
B9—B4—B860.44 (4)B7—B11—H11121.8 (5)
C3—B4—H4117.1 (5)B10—B11—H11124.6 (5)
C3—B4—B5106.09 (5)B12—B11—B759.81 (4)
C3—B4—B858.72 (4)B12—B11—B1059.98 (4)
C3—B4—B9106.16 (5)B12—B11—H11126.9 (5)
C1—B5—B459.23 (3)C2—B11—B659.90 (4)
C1—B5—H5117.9 (5)C2—B11—B759.26 (4)
C1—B5—B659.04 (4)C2—B11—B10106.10 (5)
C1—B5—B9104.97 (4)C2—B11—H11119.0 (5)
C1—B5—B10104.88 (4)C2—B11—B12105.90 (5)
B4—B5—H5118.3 (4)B7—B12—B860.11 (4)
B4—B5—B6108.43 (4)B7—B12—B9108.34 (5)
B6—B5—H5120.1 (5)B7—B12—B10108.42 (5)
B9—B5—B459.47 (4)B7—B12—B1160.16 (4)
B9—B5—H5126.8 (5)B7—B12—H12119.6 (5)
B9—B5—B6108.01 (5)B8—B12—B960.04 (4)
B10—B5—B4108.00 (5)B8—B12—B10108.27 (5)
B10—B5—H5128.1 (5)B8—B12—B11108.30 (5)
B10—B5—B659.51 (4)B8—B12—H12120.2 (5)
B10—B5—B960.45 (4)B9—B12—H12122.5 (5)
C1—B6—B257.98 (3)B10—B12—B960.22 (4)
C1—B6—B558.66 (3)B10—B12—H12123.5 (5)
C1—B6—H6116.6 (5)B11—B12—B9108.50 (5)
C1—B6—B10105.00 (5)B11—B12—B1060.24 (4)
C1—B6—B11104.74 (4)B11—B12—H12121.6 (5)
C1—B6—C257.98 (3)C1—C2—H2115.4 (5)
B2—B6—B5105.98 (4)C1—C2—B359.64 (4)
B2—B6—H6117.3 (5)C1—C2—B660.37 (4)
B2—B6—B10106.05 (5)C1—C2—B7108.80 (5)
B2—B6—B1158.56 (4)C1—C2—B11108.99 (5)
B5—B6—H6122.4 (4)B3—C2—H2115.4 (5)
B10—B6—B560.04 (4)B3—C2—B6109.85 (5)
B10—B6—H6131.0 (5)B3—C2—B760.50 (4)
B10—B6—B1160.65 (4)B3—C2—B11110.08 (5)
B11—B6—B5108.35 (5)B6—C2—H2120.7 (5)
B11—B6—H6125.8 (4)B7—C2—H2122.7 (5)
C2—B6—B5105.98 (4)B7—C2—B6111.99 (5)
C2—B6—H6117.3 (5)B11—C2—H2127.7 (5)
C2—B6—B10106.05 (5)B11—C2—B661.54 (4)
C2—B6—B1158.56 (4)B11—C2—B762.04 (4)
B2—B7—H7117.2 (5)C1—C3—B259.40 (3)
B2—B7—B8106.23 (5)C1—C3—H3115.5 (5)
B2—B7—B1158.69 (4)C1—C3—B460.47 (4)
B2—B7—B12105.64 (5)C1—C3—B7108.56 (5)
B2—B7—C359.07 (4)C1—C3—B8108.78 (5)
B3—B7—H7117.4 (5)B2—C3—H3115.5 (5)
B3—B7—B858.85 (4)B2—C3—B4109.64 (5)
B3—B7—B11106.28 (5)B2—C3—B760.44 (4)
B3—B7—B12105.81 (5)B2—C3—B8109.72 (5)
B8—B7—H7124.1 (5)B4—C3—H3120.9 (5)
B8—B7—B11108.15 (5)B7—C3—H3122.7 (5)
B11—B7—H7123.6 (5)B7—C3—B4111.79 (5)
B12—B7—H7130.0 (5)B8—C3—H3128.0 (5)
B12—B7—B860.04 (4)B8—C3—B461.40 (4)
B12—B7—B1160.03 (4)B8—C3—B761.88 (4)
C1i—C1—B2—B6−110.91 (7)B6—B2—B11—B7−140.34 (5)
C1i—C1—B2—B7143.93 (6)B6—B2—B11—B10−38.74 (5)
C1i—C1—B2—B11−150.06 (6)B6—B2—B11—B12−101.40 (5)
C1i—C1—B2—C3107.28 (6)B6—B2—C3—C1−34.85 (4)
C1i—C1—B3—B4111.21 (7)B6—B2—C3—B40.16 (6)
C1i—C1—B3—B7−143.73 (6)B6—B2—C3—B7104.67 (5)
C1i—C1—B3—B8150.53 (6)B6—B2—C3—B865.83 (6)
C1i—C1—B3—C2−107.17 (7)B6—B5—B9—B4101.20 (5)
C1i—C1—B4—B3−106.17 (7)B6—B5—B9—B863.45 (6)
C1i—C1—B4—B5114.01 (7)B6—B5—B9—B10−37.09 (4)
C1i—C1—B4—B8−143.31 (6)B6—B5—B9—B120.25 (6)
C1i—C1—B4—B9153.92 (6)B6—B5—B10—B9138.27 (5)
C1i—C1—B4—C3−106.17 (7)B6—B5—B10—B1137.71 (4)
C1i—C1—B5—B4−109.25 (7)B6—B5—B10—B12100.89 (5)
C1i—C1—B5—B6108.91 (7)B6—B10—B11—B238.98 (5)
C1i—C1—B5—B9−148.80 (6)B6—B10—B11—B7101.22 (5)
C1i—C1—B5—B10148.40 (6)B6—B10—B11—B12138.33 (5)
C1i—C1—B6—B2106.28 (7)B6—B10—B11—C238.98 (5)
C1i—C1—B6—B5−114.16 (7)B6—B10—B12—B70.18 (7)
C1i—C1—B6—B10−153.94 (6)B6—B10—B12—B863.87 (6)
C1i—C1—B6—B11143.08 (6)B6—B10—B12—B9101.23 (5)
C1i—C1—B6—C2106.28 (7)B6—B10—B12—B11−37.21 (5)
C1i—C1—C2—B3107.28 (6)B6—B11—B12—B7−101.50 (5)
C1i—C1—C2—B6−110.91 (7)B6—B11—B12—B8−64.15 (6)
C1i—C1—C2—B7143.93 (6)B6—B11—B12—B9−0.51 (7)
C1i—C1—C2—B11−150.06 (6)B6—B11—B12—B1036.88 (5)
C1i—C1—C3—B2−107.17 (7)B6—B11—C2—C138.62 (4)
C1i—C1—C3—B4111.21 (7)B6—B11—C2—B3102.30 (5)
C1i—C1—C3—B7−143.73 (6)B6—B11—C2—B7140.34 (5)
C1i—C1—C3—B8150.53 (6)B7—B2—B6—C199.79 (5)
C1—B2—B6—B5−35.18 (4)B7—B2—B6—B564.61 (6)
C1—B2—B6—B10−97.92 (5)B7—B2—B6—B101.87 (6)
C1—B2—B6—B11−137.24 (5)B7—B2—B6—B11−37.44 (5)
C1—B2—B7—B80.34 (6)B7—B2—B11—B6140.34 (5)
C1—B2—B7—B11102.03 (5)B7—B2—B11—B10101.61 (5)
C1—B2—B7—B1263.05 (6)B7—B2—B11—B1238.94 (5)
C1—B2—B7—C3−36.28 (4)B7—B2—C3—C1−139.51 (5)
C1—B2—B11—B638.62 (4)B7—B2—C3—B4−104.51 (5)
C1—B2—B11—B7−101.72 (5)B7—B2—C3—B8−38.84 (4)
C1—B2—B11—B10−0.12 (6)B7—B3—B4—C1−99.64 (5)
C1—B2—B11—B12−62.78 (6)B7—B3—B4—B5−64.68 (6)
C1—B2—C3—B435.00 (4)B7—B3—B4—B837.26 (5)
C1—B2—C3—B7139.51 (5)B7—B3—B4—B9−1.74 (6)
C1—B2—C3—B8100.68 (5)B7—B3—B8—B4−140.40 (5)
C1—B3—B4—B534.96 (4)B7—B3—B8—B9−101.77 (5)
C1—B3—B4—B8136.90 (5)B7—B3—B8—B12−38.91 (4)
C1—B3—B4—B997.90 (5)B7—B3—C2—C1139.51 (5)
C1—B3—B7—B8−101.86 (5)B7—B3—C2—B6104.67 (5)
C1—B3—B7—B11−0.17 (6)B7—B3—C2—B1138.71 (5)
C1—B3—B7—B12−62.90 (6)B7—B8—B9—B4−101.14 (5)
C1—B3—B7—C236.13 (4)B7—B8—B9—B5−63.25 (6)
C1—B3—B8—B4−38.89 (4)B7—B8—B9—B10−0.21 (6)
C1—B3—B8—B7101.51 (5)B7—B8—B9—B1236.99 (5)
C1—B3—B8—B9−0.26 (6)B7—B8—B12—B9−138.63 (5)
C1—B3—B8—B1262.60 (6)B7—B8—B12—B10−101.19 (5)
C1—B3—C2—B6−34.85 (4)B7—B8—B12—B11−37.38 (5)
C1—B3—C2—B7−139.51 (5)B7—B8—C3—C1101.51 (5)
C1—B3—C2—B11−100.80 (5)B7—B8—C3—B238.20 (4)
C1—B4—B5—B633.95 (4)B7—B8—C3—B4140.40 (5)
C1—B4—B5—B9134.43 (5)B7—B11—B12—B837.35 (5)
C1—B4—B5—B1096.94 (5)B7—B11—B12—B9100.99 (5)
C1—B4—B8—B336.82 (4)B7—B11—B12—B10138.38 (5)
C1—B4—B8—B71.54 (6)B7—B11—C2—C1−101.72 (5)
C1—B4—B8—B9−99.16 (5)B7—B11—C2—B3−38.04 (5)
C1—B4—B8—B12−61.75 (6)B7—B11—C2—B6−140.34 (5)
C1—B4—B8—C336.82 (4)B8—B3—B4—C1−136.90 (5)
C1—B4—B9—B5−39.12 (4)B8—B3—B4—B5−101.94 (5)
C1—B4—B9—B898.66 (5)B8—B3—B4—B9−39.00 (5)
C1—B4—B9—B10−1.98 (6)B8—B3—B7—B11101.70 (5)
C1—B4—B9—B1261.32 (6)B8—B3—B7—B1238.96 (5)
C1—B4—C3—B2−34.58 (4)B8—B3—B7—C2137.99 (5)
C1—B4—C3—B7−99.64 (5)B8—B3—C2—C1100.68 (5)
C1—B4—C3—B8−136.90 (5)B8—B3—C2—B665.83 (6)
C1—B5—B6—B234.89 (4)B8—B3—C2—B7−38.84 (4)
C1—B5—B6—B10134.50 (5)B8—B3—C2—B11−0.12 (6)
C1—B5—B6—B1196.43 (5)B8—B4—B5—C1−96.44 (5)
C1—B5—B6—C234.89 (4)B8—B4—B5—B6−62.49 (6)
C1—B5—B9—B439.43 (4)B8—B4—B5—B937.99 (5)
C1—B5—B9—B81.68 (6)B8—B4—B5—B100.51 (6)
C1—B5—B9—B10−98.86 (5)B8—B4—B9—B5−137.78 (5)
C1—B5—B9—B12−61.52 (6)B8—B4—B9—B10−100.64 (5)
C1—B5—B10—B6−39.26 (4)B8—B4—B9—B12−37.34 (5)
C1—B5—B10—B999.01 (5)B8—B4—C3—C1136.90 (5)
C1—B5—B10—B11−1.55 (6)B8—B4—C3—B2102.33 (5)
C1—B5—B10—B1261.62 (6)B8—B4—C3—B737.26 (5)
C1—B6—B10—B539.10 (4)B8—B7—B11—B298.33 (5)
C1—B6—B10—B91.76 (6)B8—B7—B11—B662.75 (6)
C1—B6—B10—B11−98.72 (5)B8—B7—B11—B10−0.10 (6)
C1—B6—B10—B12−61.59 (6)B8—B7—B11—B12−37.29 (5)
C1—B6—B11—B2−36.53 (4)B8—B7—B11—C298.33 (5)
C1—B6—B11—B7−1.21 (6)B8—B7—B12—B937.11 (5)
C1—B6—B11—B1099.16 (5)B8—B7—B12—B10100.93 (5)
C1—B6—B11—B1262.01 (6)B8—B7—B12—B11138.36 (5)
C1—B6—B11—C2−36.53 (4)B8—B7—C2—C10.34 (6)
C1—B6—C2—B334.55 (4)B8—B7—C2—B336.63 (4)
C1—B6—C2—B799.79 (5)B8—B7—C2—B6−64.46 (6)
C1—B6—C2—B11137.24 (5)B8—B7—C2—B11−101.69 (5)
B2—C1—B4—B5−104.06 (5)B8—B7—C3—C1−101.86 (5)
B2—C1—B4—B8−1.38 (6)B8—B7—C3—B2−137.99 (5)
B2—C1—B4—B9−64.14 (5)B8—B7—C3—B4−37.06 (5)
B2—C1—B4—C335.77 (4)B8—B9—B10—B5−100.87 (5)
B2—C1—B5—B4103.88 (5)B8—B9—B10—B6−63.29 (6)
B2—C1—B5—B6−37.96 (4)B8—B9—B10—B110.15 (6)
B2—C1—B5—B964.33 (6)B8—B9—B10—B1237.18 (5)
B2—C1—B5—B101.53 (6)B8—B9—B12—B7−37.14 (5)
B2—C1—B6—B5139.56 (5)B8—B9—B12—B10−138.31 (5)
B2—C1—B6—B1099.79 (5)B8—B9—B12—B11−100.91 (5)
B2—C1—B6—B1136.80 (4)B9—B4—B5—C1−134.43 (5)
B2—C1—C3—B4−141.62 (5)B9—B4—B5—B6−100.48 (5)
B2—C1—C3—B7−36.56 (4)B9—B4—B5—B10−37.49 (5)
B2—C1—C3—B8−102.30 (5)B9—B4—B8—B3135.98 (5)
B2—B6—B10—B599.49 (5)B9—B4—B8—B7100.70 (5)
B2—B6—B10—B962.15 (6)B9—B4—B8—B1237.40 (5)
B2—B6—B10—B11−38.33 (4)B9—B4—B8—C3135.98 (5)
B2—B6—B10—B12−1.21 (6)B9—B4—C3—C197.90 (5)
B2—B6—B11—B735.32 (5)B9—B4—C3—B263.32 (6)
B2—B6—B11—B10135.69 (5)B9—B4—C3—B7−1.74 (6)
B2—B6—B11—B1298.55 (5)B9—B4—C3—B8−39.00 (5)
B2—B7—B8—B4−1.19 (6)B9—B5—B6—C1−96.99 (5)
B2—B7—B8—B961.89 (6)B9—B5—B6—B2−62.10 (6)
B2—B7—B8—B1298.99 (5)B9—B5—B6—B1037.51 (5)
B2—B7—B8—C3−36.72 (4)B9—B5—B6—B11−0.56 (6)
B2—B7—B11—B6−35.59 (5)B9—B5—B6—C2−62.10 (6)
B2—B7—B11—B10−98.43 (5)B9—B5—B10—B6−138.27 (5)
B2—B7—B11—B12−135.62 (5)B9—B5—B10—B11−100.56 (5)
B2—B7—B12—B8−100.01 (5)B9—B5—B10—B12−37.39 (5)
B2—B7—B12—B9−62.90 (6)B9—B8—B12—B7138.63 (5)
B2—B7—B12—B100.92 (6)B9—B8—B12—B1037.44 (5)
B2—B7—B12—B1138.35 (4)B9—B8—B12—B11101.25 (5)
B2—B7—C3—C136.13 (4)B9—B8—C3—C1−0.26 (6)
B2—B7—C3—B4100.92 (5)B9—B8—C3—B2−63.56 (6)
B2—B7—C3—B8137.99 (5)B9—B8—C3—B438.64 (5)
B2—B11—B12—B7−38.68 (4)B9—B8—C3—B7−101.77 (5)
B2—B11—B12—B8−1.33 (6)B9—B10—B11—B2−62.27 (6)
B2—B11—B12—B962.31 (6)B9—B10—B11—B6−101.25 (5)
B2—B11—B12—B1099.69 (5)B9—B10—B11—B7−0.03 (6)
B3—C1—B4—B5−139.82 (5)B9—B10—B11—B1237.09 (5)
B3—C1—B4—B8−37.14 (4)B9—B10—B11—C2−62.27 (6)
B3—C1—B4—B9−99.91 (5)B9—B10—B12—B7−101.04 (5)
B3—C1—B5—B437.64 (4)B9—B10—B12—B8−37.36 (5)
B3—C1—B5—B6−104.20 (5)B9—B10—B12—B11−138.44 (5)
B3—C1—B5—B9−1.91 (6)B10—B5—B6—C1−134.50 (5)
B3—C1—B5—B10−64.71 (6)B10—B5—B6—B2−99.61 (5)
B3—C1—B6—B5103.91 (5)B10—B5—B6—B11−38.07 (5)
B3—C1—B6—B1064.13 (5)B10—B5—B6—C2−99.61 (5)
B3—C1—B6—B111.15 (6)B10—B5—B9—B4138.29 (5)
B3—C1—B6—C2−35.66 (5)B10—B5—B9—B8100.55 (5)
B3—C1—C2—B6141.81 (5)B10—B5—B9—B1237.34 (5)
B3—C1—C2—B736.65 (4)B10—B6—B11—B2−135.69 (5)
B3—C1—C2—B11102.66 (5)B10—B6—B11—B7−100.36 (5)
B3—B4—B5—C1−34.72 (4)B10—B6—B11—B12−37.14 (5)
B3—B4—B5—B6−0.77 (6)B10—B6—B11—C2−135.69 (5)
B3—B4—B5—B999.71 (5)B10—B6—C2—C1−97.92 (5)
B3—B4—B5—B1062.22 (6)B10—B6—C2—B3−63.36 (6)
B3—B4—B8—B7−35.28 (5)B10—B6—C2—B71.87 (6)
B3—B4—B8—B9−135.98 (5)B10—B6—C2—B1139.32 (5)
B3—B4—B8—B12−98.57 (5)B10—B9—B12—B7101.17 (5)
B3—B4—B9—B5−99.59 (5)B10—B9—B12—B8138.31 (5)
B3—B4—B9—B838.20 (4)B10—B9—B12—B1137.40 (5)
B3—B4—B9—B10−62.44 (6)B10—B11—B12—B7−138.38 (5)
B3—B4—B9—B120.86 (6)B10—B11—B12—B8−101.02 (5)
B3—B7—B8—B435.53 (5)B10—B11—B12—B9−37.39 (5)
B3—B7—B8—B998.61 (5)B10—B11—C2—C1−0.12 (6)
B3—B7—B8—B12135.71 (5)B10—B11—C2—B363.57 (6)
B3—B7—B11—B60.87 (6)B10—B11—C2—B6−38.74 (5)
B3—B7—B11—B10−61.97 (6)B10—B11—C2—B7101.61 (5)
B3—B7—B11—B12−99.17 (5)B11—B2—B6—C1137.24 (5)
B3—B7—B11—C236.46 (4)B11—B2—B6—B5102.05 (5)
B3—B7—B12—B8−38.40 (4)B11—B2—B6—B1039.32 (5)
B3—B7—B12—B9−1.30 (6)B11—B2—B7—B8−101.69 (5)
B3—B7—B12—B1062.53 (6)B11—B2—B7—B12−38.99 (5)
B3—B7—B12—B1199.96 (5)B11—B2—B7—C3−138.32 (5)
B3—B7—C2—C1−36.28 (4)B11—B2—C3—C1−100.80 (5)
B3—B7—C2—B6−101.08 (5)B11—B2—C3—B4−65.80 (6)
B3—B7—C2—B11−138.32 (5)B11—B2—C3—B738.71 (5)
B3—B8—B9—B4−38.79 (4)B11—B2—C3—B8−0.12 (6)
B3—B8—B9—B5−0.91 (6)B11—B6—B10—B5137.82 (5)
B3—B8—B9—B1062.14 (6)B11—B6—B10—B9100.48 (5)
B3—B8—B9—B1299.33 (5)B11—B6—B10—B1237.12 (5)
B3—B8—B12—B738.64 (4)B11—B6—C2—C1−137.24 (5)
B3—B8—B12—B9−99.99 (5)B11—B6—C2—B3−102.68 (5)
B3—B8—B12—B10−62.55 (6)B11—B6—C2—B7−37.44 (5)
B3—B8—B12—B111.26 (6)B11—B7—B8—B3−98.42 (5)
B4—C1—B2—B6105.82 (5)B11—B7—B8—B4−62.89 (6)
B4—C1—B2—B70.67 (6)B11—B7—B8—B90.19 (6)
B4—C1—B2—B1166.68 (6)B11—B7—B8—B1237.28 (5)
B4—C1—B2—C3−35.98 (5)B11—B7—B8—C3−98.42 (5)
B4—C1—B3—B7105.05 (5)B11—B7—B12—B8−138.36 (5)
B4—C1—B3—B839.32 (5)B11—B7—B12—B9−101.25 (5)
B4—C1—B3—C2141.62 (5)B11—B7—B12—B10−37.43 (5)
B4—C1—B5—B6−141.84 (5)B11—B7—C2—C1102.03 (5)
B4—C1—B5—B9−39.55 (4)B11—B7—C2—B3138.32 (5)
B4—C1—B5—B10−102.35 (5)B11—B7—C2—B637.24 (5)
B4—C1—B6—B2−102.98 (5)B11—B7—C3—C1−0.17 (6)
B4—C1—B6—B536.58 (4)B11—B7—C3—B2−36.29 (5)
B4—C1—B6—B10−3.20 (6)B11—B7—C3—B464.63 (6)
B4—C1—B6—B11−66.18 (6)B11—B7—C3—B8101.70 (5)
B4—C1—B6—C2−102.98 (5)B11—B10—B12—B737.39 (5)
B4—C1—C2—B3−35.98 (5)B11—B10—B12—B8101.08 (5)
B4—C1—C2—B6105.82 (5)B11—B10—B12—B9138.44 (5)
B4—C1—C2—B70.67 (6)B12—B7—B8—B3−135.71 (5)
B4—C1—C2—B1166.68 (6)B12—B7—B8—B4−100.17 (5)
B4—C1—C3—B2141.62 (5)B12—B7—B8—B9−37.10 (5)
B4—C1—C3—B7105.05 (5)B12—B7—B8—C3−135.71 (5)
B4—C1—C3—B839.32 (5)B12—B7—B11—B2135.62 (5)
B4—B3—B7—B8−37.06 (5)B12—B7—B11—B6100.04 (5)
B4—B3—B7—B1164.63 (6)B12—B7—B11—B1037.19 (5)
B4—B3—B7—B121.90 (6)B12—B7—B11—C2135.62 (5)
B4—B3—B7—C2100.92 (5)B12—B7—C2—C163.05 (6)
B4—B3—B8—B7140.40 (5)B12—B7—C2—B399.33 (5)
B4—B3—B8—B938.64 (5)B12—B7—C2—B6−1.75 (6)
B4—B3—B8—B12101.49 (5)B12—B7—C2—B11−38.99 (5)
B4—B3—C2—C135.00 (4)B12—B7—C3—C1−62.90 (6)
B4—B3—C2—B60.16 (6)B12—B7—C3—B2−99.02 (5)
B4—B3—C2—B7−104.51 (5)B12—B7—C3—B41.90 (6)
B4—B3—C2—B11−65.80 (6)B12—B7—C3—B838.96 (5)
B4—B5—B6—C1−34.03 (4)B12—B8—B9—B4−138.12 (5)
B4—B5—B6—B20.86 (6)B12—B8—B9—B5−100.24 (5)
B4—B5—B6—B10100.47 (5)B12—B8—B9—B10−37.19 (5)
B4—B5—B6—B1162.40 (6)B12—B8—C3—C162.60 (6)
B4—B5—B6—C20.86 (6)B12—B8—C3—B2−0.71 (6)
B4—B5—B9—B8−37.75 (5)B12—B8—C3—B4101.49 (5)
B4—B5—B9—B10−138.29 (5)B12—B8—C3—B7−38.91 (4)
B4—B5—B9—B12−100.95 (5)B12—B9—B10—B5−138.05 (5)
B4—B5—B10—B6−101.22 (5)B12—B9—B10—B6−100.47 (5)
B4—B5—B10—B937.06 (4)B12—B9—B10—B11−37.03 (5)
B4—B5—B10—B11−63.50 (6)B12—B10—B11—B2−99.36 (5)
B4—B5—B10—B12−0.33 (6)B12—B10—B11—B6−138.33 (5)
B4—B8—B9—B537.88 (5)B12—B10—B11—B7−37.12 (5)
B4—B8—B9—B10100.93 (5)B12—B10—B11—C2−99.36 (5)
B4—B8—B9—B12138.12 (5)B12—B11—C2—C1−62.78 (6)
B4—B8—B12—B7101.47 (5)B12—B11—C2—B30.90 (6)
B4—B8—B12—B9−37.16 (5)B12—B11—C2—B6−101.40 (5)
B4—B8—B12—B100.28 (7)B12—B11—C2—B738.94 (5)
B4—B8—B12—B1164.09 (6)C2—C1—B3—B4−141.62 (5)
B4—B8—C3—C1−38.89 (4)C2—C1—B3—B7−36.56 (4)
B4—B8—C3—B2−102.20 (5)C2—C1—B3—B8−102.30 (5)
B4—B8—C3—B7−140.40 (5)C2—C1—B4—B335.77 (4)
B4—B9—B10—B5−37.44 (4)C2—C1—B4—B5−104.06 (5)
B4—B9—B10—B60.14 (6)C2—C1—B4—B8−1.38 (6)
B4—B9—B10—B1163.58 (6)C2—C1—B4—B9−64.14 (5)
B4—B9—B10—B12100.61 (5)C2—C1—B5—B4103.88 (5)
B4—B9—B12—B70.27 (7)C2—C1—B5—B6−37.96 (4)
B4—B9—B12—B837.41 (5)C2—C1—B5—B964.33 (6)
B4—B9—B12—B10−100.90 (5)C2—C1—B5—B101.53 (6)
B4—B9—B12—B11−63.50 (6)C2—C1—B6—B5139.56 (5)
B5—C1—B2—B638.23 (4)C2—C1—B6—B1099.79 (5)
B5—C1—B2—B7−66.93 (6)C2—C1—B6—B1136.80 (4)
B5—C1—B2—B11−0.91 (6)C2—B3—B4—C1−34.58 (4)
B5—C1—B2—C3−103.58 (5)C2—B3—B4—B50.39 (6)
B5—C1—B3—B4−37.92 (5)C2—B3—B4—B8102.33 (5)
B5—C1—B3—B767.14 (6)C2—B3—B4—B963.32 (6)
B5—C1—B3—B81.40 (6)C2—B3—B7—B8−137.99 (5)
B5—C1—B3—C2103.70 (5)C2—B3—B7—B11−36.29 (5)
B5—C1—B4—B3139.82 (5)C2—B3—B7—B12−99.02 (5)
B5—C1—B4—B8102.68 (5)C2—B3—B8—B4−102.20 (5)
B5—C1—B4—B939.91 (4)C2—B3—B8—B738.20 (4)
B5—C1—B4—C3139.82 (5)C2—B3—B8—B9−63.56 (6)
B5—C1—B6—B2−139.56 (5)C2—B3—B8—B12−0.71 (6)
B5—C1—B6—B10−39.78 (4)C2—B6—B10—B599.49 (5)
B5—C1—B6—B11−102.76 (5)C2—B6—B10—B962.15 (6)
B5—C1—B6—C2−139.56 (5)C2—B6—B10—B11−38.33 (4)
B5—C1—C2—B3−103.58 (5)C2—B6—B10—B12−1.21 (6)
B5—C1—C2—B638.23 (4)C2—B6—B11—B735.32 (5)
B5—C1—C2—B7−66.93 (6)C2—B6—B11—B10135.69 (5)
B5—C1—C2—B11−0.91 (6)C2—B6—B11—B1298.55 (5)
B5—C1—C3—B2103.70 (5)C2—B7—B8—B3−36.72 (4)
B5—C1—C3—B4−37.92 (5)C2—B7—B8—B4−1.19 (6)
B5—C1—C3—B767.14 (6)C2—B7—B8—B961.89 (6)
B5—C1—C3—B81.40 (6)C2—B7—B8—B1298.99 (5)
B5—B4—B8—B398.09 (5)C2—B7—B11—B6−35.59 (5)
B5—B4—B8—B762.81 (6)C2—B7—B11—B10−98.43 (5)
B5—B4—B8—B9−37.89 (5)C2—B7—B11—B12−135.62 (5)
B5—B4—B8—B12−0.49 (6)C2—B7—B12—B8−100.01 (5)
B5—B4—B8—C398.09 (5)C2—B7—B12—B9−62.90 (6)
B5—B4—B9—B8137.78 (5)C2—B7—B12—B100.92 (6)
B5—B4—B9—B1037.15 (4)C2—B7—B12—B1138.35 (4)
B5—B4—B9—B12100.44 (5)C2—B11—B12—B7−38.68 (4)
B5—B4—C3—C134.96 (4)C2—B11—B12—B8−1.33 (6)
B5—B4—C3—B20.39 (6)C2—B11—B12—B962.31 (6)
B5—B4—C3—B7−64.68 (6)C2—B11—B12—B1099.69 (5)
B5—B4—C3—B8−101.94 (5)C3—C1—B2—B6141.81 (5)
B5—B6—B10—B9−37.34 (4)C3—C1—B2—B736.65 (4)
B5—B6—B10—B11−137.82 (5)C3—C1—B2—B11102.66 (5)
B5—B6—B10—B12−100.70 (5)C3—C1—B4—B5−139.82 (5)
B5—B6—B11—B2−97.88 (5)C3—C1—B4—B8−37.14 (4)
B5—B6—B11—B7−62.56 (6)C3—C1—B4—B9−99.91 (5)
B5—B6—B11—B1037.80 (5)C3—C1—B5—B437.64 (4)
B5—B6—B11—B120.66 (6)C3—C1—B5—B6−104.20 (5)
B5—B6—B11—C2−97.88 (5)C3—C1—B5—B9−1.91 (6)
B5—B6—C2—C1−35.18 (4)C3—C1—B5—B10−64.71 (6)
B5—B6—C2—B3−0.63 (6)C3—C1—B6—B2−35.66 (5)
B5—B6—C2—B764.61 (6)C3—C1—B6—B5103.91 (5)
B5—B6—C2—B11102.05 (5)C3—C1—B6—B1064.13 (5)
B5—B9—B10—B637.58 (4)C3—C1—B6—B111.15 (6)
B5—B9—B10—B11101.02 (5)C3—B2—B6—C134.55 (4)
B5—B9—B10—B12138.05 (5)C3—B2—B6—B5−0.63 (6)
B5—B9—B12—B763.94 (6)C3—B2—B6—B10−63.36 (6)
B5—B9—B12—B8101.08 (5)C3—B2—B6—B11−102.68 (5)
B5—B9—B12—B10−37.23 (5)C3—B2—B7—B836.63 (4)
B5—B9—B12—B110.16 (7)C3—B2—B7—B11138.32 (5)
B5—B10—B11—B21.05 (6)C3—B2—B7—B1299.33 (5)
B5—B10—B11—B6−37.93 (4)C3—B2—B11—B6102.30 (5)
B5—B10—B11—B763.29 (6)C3—B2—B11—B7−38.04 (5)
B5—B10—B11—B12100.41 (5)C3—B2—B11—B1063.57 (6)
B5—B10—B11—C21.05 (6)C3—B2—B11—B120.90 (6)
B5—B10—B12—B7−63.66 (6)C3—B4—B5—C1−34.72 (4)
B5—B10—B12—B80.03 (7)C3—B4—B5—B6−0.77 (6)
B5—B10—B12—B937.39 (5)C3—B4—B5—B999.71 (5)
B5—B10—B12—B11−101.05 (5)C3—B4—B5—B1062.22 (6)
B6—C1—B2—B7−105.16 (5)C3—B4—B8—B7−35.28 (5)
B6—C1—B2—B11−39.15 (5)C3—B4—B8—B9−135.98 (5)
B6—C1—B2—C3−141.81 (5)C3—B4—B8—B12−98.57 (5)
B6—C1—B3—B4−105.69 (5)C3—B4—B9—B5−99.59 (5)
B6—C1—B3—B7−0.63 (6)C3—B4—B9—B838.20 (4)
B6—C1—B3—B8−66.37 (6)C3—B4—B9—B10−62.44 (6)
B6—C1—B3—C235.93 (5)C3—B4—B9—B120.86 (6)
B6—C1—B4—B3103.20 (5)C3—B7—B8—B435.53 (5)
B6—C1—B4—B5−36.63 (4)C3—B7—B8—B998.61 (5)
B6—C1—B4—B866.05 (6)C3—B7—B8—B12135.71 (5)
B6—C1—B4—B93.29 (6)C3—B7—B11—B236.46 (4)
B6—C1—B4—C3103.20 (5)C3—B7—B11—B60.87 (6)
B6—C1—B5—B4141.84 (5)C3—B7—B11—B10−61.97 (6)
B6—C1—B5—B9102.29 (5)C3—B7—B11—B12−99.17 (5)
B6—C1—B5—B1039.49 (4)C3—B7—B12—B8−38.40 (4)
B6—C1—C2—B3−141.81 (5)C3—B7—B12—B9−1.30 (6)
B6—C1—C2—B7−105.16 (5)C3—B7—B12—B1062.53 (6)
B6—C1—C2—B11−39.15 (5)C3—B7—B12—B1199.96 (5)
B6—C1—C3—B235.93 (5)C3—B8—B9—B4−38.79 (4)
B6—C1—C3—B4−105.69 (5)C3—B8—B9—B5−0.91 (6)
B6—C1—C3—B7−0.63 (6)C3—B8—B9—B1062.14 (6)
B6—C1—C3—B8−66.37 (6)C3—B8—B9—B1299.33 (5)
B6—B2—B7—B8−64.46 (6)C3—B8—B12—B738.64 (4)
B6—B2—B7—B1137.24 (5)C3—B8—B12—B9−99.99 (5)
B6—B2—B7—B12−1.75 (6)C3—B8—B12—B10−62.55 (6)
B6—B2—B7—C3−101.08 (5)C3—B8—B12—B111.26 (6)
  7 in total

1.  Structural Characterization of Representative d(7), d(8), and d(9) Transition Metal Complexes of Bis(o-carborane).

Authors:  David E. Harwell; Jeffrey McMillan; Carolyn B. Knobler; M. Frederick Hawthorne
Journal:  Inorg Chem       Date:  1997-12-03       Impact factor: 5.165

2.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

3.  The Cambridge Structural Database in retrospect and prospect.

Authors:  Colin R Groom; Frank H Allen
Journal:  Angew Chem Int Ed Engl       Date:  2014-01-02       Impact factor: 15.336

4.  Asymmetric 1,8/13,2,x-M2C2B10 14-vertex metallacarboranes by direct electrophilic insertion reactions; the VCD and BHD methods in critical analysis of cage C atom positions.

Authors:  Amelia McAnaw; Maria Elena Lopez; David Ellis; Georgina M Rosair; Alan J Welch
Journal:  Dalton Trans       Date:  2014-04-07       Impact factor: 4.390

5.  Room-temperature C-C bond cleavage of an arene by a metallacarborane.

Authors:  David Ellis; David McKay; Stuart A Macgregor; Georgina M Rosair; Alan J Welch
Journal:  Angew Chem Int Ed Engl       Date:  2010-07-05       Impact factor: 15.336

6.  The first supraicosahedral bis(heteroborane).

Authors:  David Ellis; Georgina M Rosair; Alan J Welch
Journal:  Chem Commun (Camb)       Date:  2010-09-07       Impact factor: 6.222

7.  The VCD method--a simple and reliable way to distinguish cage C and B atoms in (hetero)carborane structures determined crystallographically.

Authors:  Amelia McAnaw; Greig Scott; Lisa Elrick; Georgina M Rosair; Alan J Welch
Journal:  Dalton Trans       Date:  2013-01-21       Impact factor: 4.390

  7 in total

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