Reaction of R(Ph)SnCl 2(R=Me, Et) with 2,6-diacetylpyridine bis(thiosemicarbazone) (H 2DAPTSC): the crystal structures of [Me(Ph)Sn(HDAPTSC)]Cl · 1.25 MeOH and [Et(Ph)Sn(H 2DAPTSC)]Cl 2 · MeOH · H 2O
Complexes of R(Ph)SnCl 2 (R=Me, Et) with 2,6-diacetylpyridine bis(thiosemicarbazone) have been synthesized and characterized by X-ray crystallography, 1H and 119Sn NMR spectroscopy and conductivity measurements. The crystal structures of [Me(Ph)Sn(HDAPTSC)]Cl · 1.25MeOH ( 1) and [Et(Ph)Sn(H 2DAPTSC)...
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Published in | Inorganica Chimica Acta Vol. 357; no. 8; pp. 2324 - 2330 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
2004
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Subjects | |
Online Access | Get full text |
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Summary: | Complexes of R(Ph)SnCl
2 (R=Me, Et) with 2,6-diacetylpyridine bis(thiosemicarbazone) have been synthesized and characterized by X-ray crystallography,
1H and
119Sn NMR spectroscopy and conductivity measurements. The crystal structures of [Me(Ph)Sn(HDAPTSC)]Cl
·
1.25MeOH (
1) and [Et(Ph)Sn(H
2DAPTSC)]Cl
2
·
MeOH
·
H
2O (
2) contain the ligand, monodeprotonated or neutral, acting as pentadentate. NMR studies in DMSO solution suggest the total dissociation of (
2), whereas (
1) evolves to form the new complex [Me(Ph)Sn(DAPTSC)].
The reactions of Me(Ph)SnCl
2 and Et(Ph)SnCl
2 with 2,6-diacetylpyridine bis(thiosemicarbazone) (H
2DAPTSC) afforded the complexes [Me(Ph)Sn(HDAPTSC)]Cl
·
1.25MeOH (
1) and [Et(Ph)Sn(H
2DAPTSC)]Cl
2
·
MeOH
·
H
2O (
2), respectively. Single-crystal X-ray crystallography showed that in both complexes the ligand, monodeprotonated in
1 and neutral in
2, is S(1),S(2),N(3),N(4),N(5)-coordinated, and the coordination geometry around the metal can be described as a distorted pentagonal bipyramid with the aryl and alkyl groups in axial positions.
1H and
119Sn NMR studies of solution in DMSO suggest that
2 dissociates completely in this solvent, while
1 evolves to the new complex [Me(Ph)Sn(DAPTSC)], with release of H
2DAPTSC and Me(Ph)SnCl
2. These conclusions were also supported by conductivity measurements. |
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ISSN: | 0020-1693 1873-3255 |
DOI: | 10.1016/j.ica.2004.01.014 |