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Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation, Biological Evaluation, Structural Elucidation Based upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies
Stable, six coordinated Bu(2)SnLA type complexes have been prepared [where LH = RCOC:C(OH)N(C(6) H(5))N:CCH(3); R = -4-F-C(6)H(4)-(L(1)H), R = -4-Cl-C(6)H(4)-(L(2)H), R= -4-Br-C(6)H(4)-(L(3)H), R=-CF(3)(L(4)H) and AH = C(O)C(6) H(4) C(O)NCHR'COOH; R'= -H(A(1)H), -CH(3)(A(2)H), -CH(CH(3))(2...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267094/ https://www.ncbi.nlm.nih.gov/pubmed/18365100 http://dx.doi.org/10.1155/BCA.2005.201 |
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author | Joshi, Anurag Verma, Shashi Gaurb, R. B. Sharma, R. R. |
author_facet | Joshi, Anurag Verma, Shashi Gaurb, R. B. Sharma, R. R. |
author_sort | Joshi, Anurag |
collection | PubMed |
description | Stable, six coordinated Bu(2)SnLA type complexes have been prepared [where LH = RCOC:C(OH)N(C(6) H(5))N:CCH(3); R = -4-F-C(6)H(4)-(L(1)H), R = -4-Cl-C(6)H(4)-(L(2)H), R= -4-Br-C(6)H(4)-(L(3)H), R=-CF(3)(L(4)H) and AH = C(O)C(6) H(4) C(O)NCHR'COOH; R'= -H(A(1)H), -CH(3)(A(2)H), -CH(CH(3))(2)(A(3)H)] by the interaction of 1:1:1 molar ratios of di-n-butyltin(IV) dichloride with corresponding organic moieties in refluxing benzene using two moles of Et(3)N as a base. In these complexes LH and AH behave as bidentate and coordination is taking place through oxygen, this is inferred from IR and (13)C NMR studies. These complexes possess tin atoms in skew trapezoidal bipyramidal geometry with the C-Sn-C angles ranging from 149.88(°) to 156.84(°). Some of these complexes with their corresponding organic moieties (LH, AH) were tested for their antimicrobial activities. |
format | Text |
id | pubmed-2267094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-22670942008-03-24 Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation, Biological Evaluation, Structural Elucidation Based upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies Joshi, Anurag Verma, Shashi Gaurb, R. B. Sharma, R. R. Bioinorg Chem Appl Research Article Stable, six coordinated Bu(2)SnLA type complexes have been prepared [where LH = RCOC:C(OH)N(C(6) H(5))N:CCH(3); R = -4-F-C(6)H(4)-(L(1)H), R = -4-Cl-C(6)H(4)-(L(2)H), R= -4-Br-C(6)H(4)-(L(3)H), R=-CF(3)(L(4)H) and AH = C(O)C(6) H(4) C(O)NCHR'COOH; R'= -H(A(1)H), -CH(3)(A(2)H), -CH(CH(3))(2)(A(3)H)] by the interaction of 1:1:1 molar ratios of di-n-butyltin(IV) dichloride with corresponding organic moieties in refluxing benzene using two moles of Et(3)N as a base. In these complexes LH and AH behave as bidentate and coordination is taking place through oxygen, this is inferred from IR and (13)C NMR studies. These complexes possess tin atoms in skew trapezoidal bipyramidal geometry with the C-Sn-C angles ranging from 149.88(°) to 156.84(°). Some of these complexes with their corresponding organic moieties (LH, AH) were tested for their antimicrobial activities. Hindawi Publishing Corporation 2005 /pmc/articles/PMC2267094/ /pubmed/18365100 http://dx.doi.org/10.1155/BCA.2005.201 Text en Copyright © 2005 Anurag Joshi et al. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Joshi, Anurag Verma, Shashi Gaurb, R. B. Sharma, R. R. Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation, Biological Evaluation, Structural Elucidation Based upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies |
title | Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation,
Biological Evaluation, Structural Elucidation Based
upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies |
title_full | Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation,
Biological Evaluation, Structural Elucidation Based
upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies |
title_fullStr | Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation,
Biological Evaluation, Structural Elucidation Based
upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies |
title_full_unstemmed | Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation,
Biological Evaluation, Structural Elucidation Based
upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies |
title_short | Di-n-butyltin(IV) Complexes Derived from Heterocyclic β-diketones and N-Phthaloyl Amino Acids: Preparation,
Biological Evaluation, Structural Elucidation Based
upon Spectral [IR, NMR ((1)H, (13)C, (19)F and (119)Sn)] Studies |
title_sort | di-n-butyltin(iv) complexes derived from heterocyclic β-diketones and n-phthaloyl amino acids: preparation,
biological evaluation, structural elucidation based
upon spectral [ir, nmr ((1)h, (13)c, (19)f and (119)sn)] studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267094/ https://www.ncbi.nlm.nih.gov/pubmed/18365100 http://dx.doi.org/10.1155/BCA.2005.201 |
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