2011
DOI: 10.1016/j.jorganchem.2010.11.029
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Chiral organotin (IV) carboxylates complexes: Syntheses, characterization, and crystal structures with chiral (S)-(+)-6-methoxy-α-methyl-2-naphthaleneaceto acid ligand

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Cited by 18 publications
(16 citation statements)
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“…2.282 Å ) and 2.101-2.131 Å (av. 2.113 Å ), which is consistent with those reported for other triorganotin carboxylates[39].…”
supporting
confidence: 91%
“…2.282 Å ) and 2.101-2.131 Å (av. 2.113 Å ), which is consistent with those reported for other triorganotin carboxylates[39].…”
supporting
confidence: 91%
“…The band at 3486 cm -1 which appeared in the free ligand as the υ(O-H) stretching vibrations but absent in compounds 1-4, indicated metalligand bond formation through these sites [25]. The red shifts of the bands with respect to the free acid also served to confirm the formation of organotin carboxylates [10]. The binding mode of ligand to tin atom was determined by the difference between the asymmetric and symmetric carboxylate stretching vibrations, Δυ = υ asym (COO) and υ sym (COO) [26].…”
Section: = Hooccookmentioning
confidence: 94%
“…The high coordination ability of tin, especially its ability to participate either in weak or strong intra or intermolecular coordination [6], has given organotin (IV) chemistry wide recognition. Tin compounds have a fascinating solution and solid phase chemistry [7]. The coordination characteristics of tin and the structures differ dramatically in solution and in solid state when a nucleophilic group is present in the tin moiety or when an organic group is linked by a Sn─C bond [8] and bears additional functionality with donor properties due to the presence of O, N and S as donor atoms [2]- [6].…”
Section: Introductionmentioning
confidence: 99%
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