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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 ]
... Helv. Chim. Acta (1982), 65, 1547-1554]. (13)See L. Norskov-Lauritsen, H.-B. Bürgi, P. Hoffmann & H. R. ... Chim. Acta (1982), 65, 1555-1562]. (15)See J. L. Hencher (1978). [In The chemistry of the CC triple ... Am. Chem. Soc. (1983), 105, 2776-2783]. (26) See L. Lebioda [Acta Cryst. (1980), B36, 271-275]. (27) ...

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 ]
... k (1986). J. Organomet. Chem. 304, 41-82. (7) L. F. Larkworthy, K. B. Nolan & P. O'Brien (1987). ... chemistry, Vol. 4, pp. 635-900. London: Pergamon Press. (9) L. Sacconi, F. Mani & A. Bencini (1987). Comprehensive coordination chemistry ... Adv. Organomet. Chem. 22, 1-58. (35) M. Tachikawa & E. L. Muetterties (1981). Prog. Inorg. Chem. 28, 203-238. ( ...

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 ]
Discussion 9.6.4. Discussion Table 9.6.3.3 has been derived from the CSD, and, as a result, does not contain every precisely determined metal-ligand interatomic distance. For example, there are many ammine (M-NH3), carbonyl (M-CO), halide (M-Cl etc.), and aqua (M-OH2) complexes that do not fall within the ...

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 ]
Statistics 9.6.2.4. Statistics Where there are less than four independent observations of a given bond length, then each individual observation is given explicitly in Table 9.6.3.3. In all other cases, the following statistics were generated by the program STATS. (i) The unweighted sample mean, d, where and is the ith observation ...
     [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 ]
... Pergamon Press. Harmony, M. D., Laurie, R. W., Kuczkowski, R. L., Schwendemann, R. H., Ramsay, D. A., Lovas, F. J., Lafferty ... chemistry, pp. 427-525. London: Royal Society of Chemistry. Sutton, L. E. (1958). Tables of interatomic distances and configuration in ... and ions. Spec. Publ. No. 11. London: Chemical Society. Sutton, L. E. (1965). Tables of interatomic distances and configuration ...

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 ]
... Helv. Chim. Acta (1982), 65, 1547-1554]. (13)See L. Norskov-Lauritsen, H.-B. Bürgi, P. Hoffmann & H. R. ... Chim. Acta (1982), 65, 1555-1562]. (15)See J. L. Hencher (1978). [In The chemistry of the CC triple ... Am. Chem. Soc. (1983), 105, 2776-2783]. (26) See L. Lebioda [Acta Cryst. (1980), B36, 271-275]. (27) ...

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 ]
Discussion 9.5.4. Discussion It should be remembered that this table has been derived from the organic section of CSD. We are aware that a number of organic bond types which occur very frequently in organometallics and metal complexes (e.g. CC in cyclopentadienyl, C-P in triphenylphosphine, etc.) are either absent or ...

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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