Catalyzed substitutions on cationic palladium(II) complexes. III. Mercury(II) catalyzed displacement of coordinated thiocyanate and selenocyanate linkage isomers
A kinetic study of Hg 2+ catalyzed solvolysis of linkage isomers [Pd(AAA)XCN/NCX] + (AAA = 1,1,7,7-tetraethyldiethylenetriamine (Et 4dien) and 4-methyl-1,1,7,7-tetraethydiethylenetriamine (MeEt 4dien); X = S, Se) has been carried out in methanol at 25 °C. The kinetic results show that the catalytic...
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Published in | Inorganica Chimica Acta Vol. 30; pp. 29 - 34 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
1978
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Abstract | A kinetic study of Hg
2+ catalyzed solvolysis of linkage isomers [Pd(AAA)XCN/NCX]
+ (AAA = 1,1,7,7-tetraethyldiethylenetriamine (Et
4dien) and 4-methyl-1,1,7,7-tetraethydiethylenetriamine (MeEt
4dien); X = S, Se) has been carried out in methanol at 25 °C. The kinetic results show that the catalytic efficiency of mercury(II) in removing the thiocyanate or selenocyanate ligands is greater in the PdXCN substrates than in the PdNCX ones, depending on whether the sulfur or selenium atom on which the attack by Hg
2+ takes place, is bonded directly to palladium(II). The kinetic data for the isomerization and substitution reactions are also reported. |
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AbstractList | A kinetic study of Hg
2+ catalyzed solvolysis of linkage isomers [Pd(AAA)XCN/NCX]
+ (AAA = 1,1,7,7-tetraethyldiethylenetriamine (Et
4dien) and 4-methyl-1,1,7,7-tetraethydiethylenetriamine (MeEt
4dien); X = S, Se) has been carried out in methanol at 25 °C. The kinetic results show that the catalytic efficiency of mercury(II) in removing the thiocyanate or selenocyanate ligands is greater in the PdXCN substrates than in the PdNCX ones, depending on whether the sulfur or selenium atom on which the attack by Hg
2+ takes place, is bonded directly to palladium(II). The kinetic data for the isomerization and substitution reactions are also reported. |
Author | Guglielmo, G. Cusumano, M. Ricevuto, V. Marricchi, P. |
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CitedBy_id | crossref_primary_10_1002_chin_197850321 crossref_primary_10_1007_BF01022335 crossref_primary_10_1007_s11243_014_9805_1 crossref_primary_10_1016_j_poly_2012_12_009 crossref_primary_10_1021_ic000320j crossref_primary_10_1016_0010_8545_85_80033_3 |
Cites_doi | 10.1021/ja00965a013 10.1021/ic50063a019 10.1021/ja00959a063 10.1021/ic50056a011 10.1021/ic50119a030 10.1021/ja01029a009 10.1021/ic50038a041 10.1021/ic50029a044 10.1016/S0020-1693(00)81955-6 10.1021/ic50096a001 10.1039/J19670001884 10.1016/S0020-1693(00)85734-5 10.1016/S0020-1693(00)85697-2 10.1016/S0020-1693(00)89877-1 10.1016/S0020-1693(00)91702-X 10.1021/ja01018a017 10.1021/ic50063a014 10.1021/ic50087a003 10.1021/ic50047a013 10.1021/ic50115a022 10.1021/ic50086a008 10.1016/S0010-8545(00)80009-0 |
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Snippet | A kinetic study of Hg
2+ catalyzed solvolysis of linkage isomers [Pd(AAA)XCN/NCX]
+ (AAA = 1,1,7,7-tetraethyldiethylenetriamine (Et
4dien) and... |
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Title | Catalyzed substitutions on cationic palladium(II) complexes. III. Mercury(II) catalyzed displacement of coordinated thiocyanate and selenocyanate linkage isomers |
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