1989
DOI: 10.1016/0022-328x(89)87171-2
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The crystal structure of dimethylphenyltin(IV) acetate

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Cited by 24 publications
(12 citation statements)
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“…The tin-oxygen bond lengths of 2.2231(2) and 2.3800(2) Å is attributed to the unevenness in bonding; the latter value is in the range of Sn-O bond lengths, which have been reported for intramolecular bonds in triorganotin carboxylates [47]. The intramolecular tin-oxygen bond length [Sn(1)-O(2), 2.3800 Å ] is similar to those of trimethyltin(IV) and dimethylphenyltin(IV) acetates [24,48] but is slightly longer than that of triphenyltin acetate(IV) [49]. Although the oxygen-tin-oxygen skeleton is bent, 164.08 (7) [35] is probably imposed by anthracene group to minimize steric interactions.…”
Section: Nmr Spectroscopysupporting
confidence: 54%
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“…The tin-oxygen bond lengths of 2.2231(2) and 2.3800(2) Å is attributed to the unevenness in bonding; the latter value is in the range of Sn-O bond lengths, which have been reported for intramolecular bonds in triorganotin carboxylates [47]. The intramolecular tin-oxygen bond length [Sn(1)-O(2), 2.3800 Å ] is similar to those of trimethyltin(IV) and dimethylphenyltin(IV) acetates [24,48] but is slightly longer than that of triphenyltin acetate(IV) [49]. Although the oxygen-tin-oxygen skeleton is bent, 164.08 (7) [35] is probably imposed by anthracene group to minimize steric interactions.…”
Section: Nmr Spectroscopysupporting
confidence: 54%
“…Several authors have used various approaches for synthesis of organotin carboxylates, including reacting organotin chloride to carboxylic acid in the presence of sodium hydroxide or sodium salt of carboxylic acids. Alternatively, they were prepared by reacting organotin iodide to silver acetates [24]. However, in the latter approach, cleavage of aryl groups present some difficulties, consequently a milder synthetic approach has been used.…”
Section: Synthesismentioning
confidence: 99%
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“…Among them, the study of the structural chemistry of triorganotin carboxylates has received considerable attention owing to the various structural types that may be adopted in the solid state [12][13][14][15][16][17][18][19]. Although a large number of structural studies have been carried out on the triorganostannyl esters of monofunctional carboxylic acids [20], relatively little work has so far been undertaken on the triorganotin esters of dicarboxylic acids [21][22][23][24].…”
Section: Introductionmentioning
confidence: 99%
“…A central question in the structural chemistry of triorganotin(IV) carboxylates is whether carboxylate groups will chelate to form monomers with four-coordinate tin or give five-coordinate polymers as a result of carboxylate bridging (Amini, Ng, Fidelis, Heeg, Muchmore, van der Helm & Zuckerman, 1989). Triphenyltin(IV) arylcarboxylates are generally monomeric molecules with tetrahedral tin (Ng, Kumar Das, van Meurs, Schagen & Strayer, 1989); the aryl group prefers to be conjugated to the carboxylate group and to be coplanar with it.…”
Section: Introductionmentioning
confidence: 99%