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Typical interatomic distances: organic compounds
Allen, F. H., Watson, D. G., Brammer, L., Orpen, A. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, ch. 9.5, pp. 790-811 [ doi:10.1107/97809553602060000621 ]
... were included on the basis of either (a) the crystallographic R factor was 0.07 and the reported mean estimated standard deviation ... 1 or 2 in the CSD), or (b) the crystallographic R factor 0.05 and the mean e.s.d. for C-C bonds ... length in a total sample of n observations. Recent work (Taylor & Kennard, 1983, 1985, 1986) has shown that the unweighted ...

Typical interatomic distances: organometallic compounds and coordination complexes of the d- and f-block metals
Orpen, A. G., Brammer, L., Allen, F. H., Watson, D. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, ch. 9.6, pp. 812-896 [ doi:10.1107/97809553602060000622 ]
... or I atoms of the ligands. (1) T. J. Marks & R. D. Ernst (1982). Comprehensive organometallic chemistry, Vol. 3, pp. ... 699-969. London: Pergamon Press. (8) D. A. Buckingham & C. R. Clark (1987). Comprehensive coordination chemistry, Vol. 4, pp. 635 ... pp. 1255-1319. London: Pergamon Press. (25) M. Melník & R. V. Parrish (1986). Coord. Chem. Rev. 70, 157- ...

Discussion
Orpen, A. G., Brammer, L., Allen, F. H., Watson, D. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, Section 9.6.4, pp. 818-884 [ doi:10.1107/97809553602060000622 ]
... the distributions represented in Table 9.6.3.3. References Bergerhoff, G., Hundt, R., Sievers, R. & Brown, I. D. (1983). The Inorganic Crystal Structure Database. ...

Use of the `Note' column
Orpen, A. G., Brammer, L., Allen, F. H., Watson, D. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, Section 9.6.3.3, pp. 817-818 [ doi:10.1107/97809553602060000622 ]
Use of the `Note' column 9.6.3.3. Use of the `Note' column The `Note' column refers to the footnotes collected in Appendix 9.6.1. These record additional information as follows: (a) notable features of the distribution of distances, e.g. likely bias due to dominance by one structure of substructure, skewness, bimodality (subdivisions of ...
     [more results from section 9.6.3 in volume C]

Statistics
Orpen, A. G., Brammer, L., Allen, F. H., Watson, D. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, Section 9.6.2.4, pp. 813-814 [ doi:10.1107/97809553602060000622 ]
... length in a total sample of n observations. Recent work (Taylor & Kennard, 1983, 1985, 1986) has shown that the unweighted mean ... Jahn-Teller effects) on the structures of copper complexes. References Taylor, R. & Kennard, O. (1983). The estimation of average molecular ...
     [more results from section 9.6.2 in volume C]

Introduction
Orpen, A. G., Brammer, L., Allen, F. H., Watson, D. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, Section 9.6.1, p. 812 [ doi:10.1107/97809553602060000622 ]
... B. G., Kennard, O., Motherwell, W. D. S., Rodgers, J. R. & Watson, D. G. (1979). The Cambridge Crystallographic Data Centre ... pp. 1209-1520. London: Pergamon Press. Harmony, M. D., Laurie, R. W., Kuczkowski, R. L., Schwendemann, R. H., Ramsay, D. A., Lovas, F. ...

Typical interatomic distances: organic compounds
Allen, F. H., Watson, D. G., Brammer, L., Orpen, A. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, ch. 9.5, pp. 790-811 [ doi:10.1107/97809553602060000621 ]
Typical interatomic distances: organic compounds Mean bond lengths for organic compounds, derived from the Cambridge Structural Database, are tabulated for 625 different bond types involving the elements C, H, N, O, B, F, P, S, Cl, As, Se, Br, Te and I. Associated statistical information characterizes each of the distributions, which ...

Typical interatomic distances: organic compounds
Allen, F. H., Watson, D. G., Brammer, L., Orpen, A. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, ch. 9.5, pp. 790-811 [ doi:10.1107/97809553602060000621 ]
... Nsp2 coplanar ([tau]BN = 0 ± 15°) predominates. See G. Schmidt, R. Boese & D. Bläser [Z. Naturforsch. Teil B (1982), 37 ... L. Norskov-Lauritsen, H.-B. Bürgi, P. Hoffmann & H. R. Schmidt [Helv. Chim. Acta (1985), 68, 76-82]. (14 ... is >= 117.5°. (24) Cyclic and acyclic peptides. (25) See R. H. Blessing [J. Am. Chem. Soc. (1983), 105, 2776- ...

Discussion
Allen, F. H., Watson, D. G., Brammer, L., Orpen, A. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, Section 9.5.4, p. 794 [ doi:10.1107/97809553602060000621 ]
... hydrogen bonds and non-bonded interactions. References Bergerhoff, G., Hundt, R., Sievers, R. & Brown, I. D. (1983). The Inorganic Crystal Structure Database. ...

Use of the `Note' column
Allen, F. H., Watson, D. G., Brammer, L., Orpen, A. G. and Taylor, R.  International Tables for Crystallography (2006). Vol. C, Section 9.5.3.3, pp. 793-794 [ doi:10.1107/97809553602060000621 ]
Use of the `Note' column 9.5.3.3. Use of the `Note' column The `Note' column refers to the footnotes collected in Appendix 9.5.1. These record additional information as follows: (a) additional details concerning the chemical definition of substructures, e.g. the omission of three- and four-membered rings; (b) statements of geometrical constraints ...
     [more results from section 9.5.3 in volume C]

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