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64349091464
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· of nitrogen (1.55 A) and iodine (1.98 A), respectively.
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· of nitrogen (1.55 A) and iodine (1.98 A), respectively.
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The methyl hydrogen atom forms shorter C-H · · · π(CN) hydrogen bonds (H· · · N 2.255 Å; H · · · C 2.398 Å) than the ring hydrogen atom (H · · · N 2.713 Å; H · · · C 2.708 Å).
-
(a) The methyl hydrogen atom forms shorter C-H · · · π(CN) hydrogen bonds (H· · · N 2.255 Å; H · · · C 2.398 Å) than the ring hydrogen atom (H · · · N 2.713 Å; H · · · C 2.708 Å).
-
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58
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64349090175
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In addition to the halogen bonds and hydrogen bonds observed here, simple Lewis acids such as alkali metal cations have been shown to interact side-on with coordinated cyanide ligands, i.e, with the C=N bond rather than the nitrogen lone pair, see refs 8a and 8e
-
(b) In addition to the halogen bonds and hydrogen bonds observed here, simple Lewis acids such as alkali metal cations have been shown to interact side-on with coordinated cyanide ligands, i.e., with the C=N bond rather than the nitrogen lone pair, see refs 8a and 8e.
-
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59
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64349116668
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HI 0.99).
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HI 0.99).
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61
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64349101023
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Geometric restrictions on the database search were X · · · O <3.5 Å and C-X · · · O ≥ 140°.
-
(b) Geometric restrictions on the database search were X · · · O <3.5 Å and C-X · · · O ≥ 140°.
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We note that there is no evidence for an additional [Ru(4,4′- tBu2-bipy)(CN)4]2- → pyridinium charge-transfer band, which might be expected, cf. the titration of hexacyanoferrate(II) with a pyridinium cation which generated a hexacyanoferrate(II) → pyridinium charge-transfer transition at the blue end of the visible region of the spectrum (ref 21, However, this CT transition was weak (ε, 41 M-1 cm-1, and such a transition would be obscured by the MLCT transitions associated with the [Ru(4,4′-tBu2-bipy)(CN)4]2- complex which are two orders of magnitude more intense
-
2- complex which are two orders of magnitude more intense.
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