Reactivity of neutral nitrogen donors in planar d8metal complexes. Part 2. The system [2,6-bis(methylsulfanyl-methyl)pyridine]chloroplatinum(II) with pyridines and amines in methanol. Effect of basicity, π-acceptor capacity and steric hindrance
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1994/DT/DT9940003539
Reference24 articles.
1. Reactivity of neutral nitrogen donors in planar d8 metal complexes. Part 1. The system [1,2-bis(phenylsulfanyl)-ethane]dichloroplatinum(II) with pyridines in methanol. Effect of basicity and steric hindrance
2. Nucleophilic reactivity constants toward methyl iodide and trans-dichlorodi(pyridine)platinum(II)
3. Nucleophilic discrimination and the trans effect. The kinetics of displacement of X from trans-[Pt(L)(X)Cl2] n? (L = Me2SO, Et2S, PMe3, PEt3, PPh3, or AsEt3; X = Cl, n= 1; X = MeOH, n= 0) by neutral and anionic nucleophiles
4. Kinetics of the displacement of chloride by amine under the trans effect of dimethyl sulfide in square-planar platinum(II) complexes
5. Nucleophilic reactivity in substitution reactions at planar tetra-coordinate monocationic platinum(II) complexes. Kinetics of displacement of chloride from chloro[2,6-bis(methylthiomethyl)pyridine]platinum(II) cation
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