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Design, synthesis and properties of orthopalladated complexes: proheterogeneous catalyst

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Resumo:The reaction of multidentate ligand, 3 ((E) (2 ((E) 4 aryldiazenyl)phenylimino)methyl)benzene 1,2 diol, H2L (H2L1, 1a; H2L2, 1b and H2L3, 1c) and (E) 2 ((2 (aryldiazenyl)phenylamino)methyl)phenol, HA (HA1, 3a; HA2, 3b and HA3, 3c) [where H represents the dissociable protons upon complexation, and aryl groups of H2L and HA are phenyl for H2L1 and HA1, p methylphenyl for H2L2 and HA2, and p chlorophenyl for H2L3 and HA3], with Na2PdCl4 separately afforded orthometallated complexes [(L)Pd], (2a, 2b and 2c) and [(A)PdCl] (4a, 4b and 4c) respectively. In the case of [(L)Pd], the deprotonated L2 ligands bind pal ladium (II) in a tetradentate (C,N,N,O) fashion whereas in the case of [(A)PdCl], the deprotonated A ligands bind Pd(II) in tridentate (C,N,N) manner. X ray structures of [(L1)Pd], (2a) and [(A1)PdCl] (4a) were determined to confirm the molecular structures. Both the complexes 4a and 5a exhibited catalytic activ ity toward Suzuki and Heck reactions. Conversion of [(A)PdCl] to its oxidized form upon ligand oxidation is reported.
Autores principais:Das, Uttam
Outros Autores:Pattanayak, Poulami; Patra, Debprasad; Brandão, Paula; Felix, Vitor; Chattopadhyay, Surajit
Assunto:Orthopalladation Crystal structure Oxidation reaction Suzuki and Heck reactions Proheterogeneous catalyst
Ano:2016
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso restrito
Instituição associada:Universidade de Aveiro
Idioma:inglês
Origem:RIA - Repositório Institucional da Universidade de Aveiro
Descrição
Resumo:The reaction of multidentate ligand, 3 ((E) (2 ((E) 4 aryldiazenyl)phenylimino)methyl)benzene 1,2 diol, H2L (H2L1, 1a; H2L2, 1b and H2L3, 1c) and (E) 2 ((2 (aryldiazenyl)phenylamino)methyl)phenol, HA (HA1, 3a; HA2, 3b and HA3, 3c) [where H represents the dissociable protons upon complexation, and aryl groups of H2L and HA are phenyl for H2L1 and HA1, p methylphenyl for H2L2 and HA2, and p chlorophenyl for H2L3 and HA3], with Na2PdCl4 separately afforded orthometallated complexes [(L)Pd], (2a, 2b and 2c) and [(A)PdCl] (4a, 4b and 4c) respectively. In the case of [(L)Pd], the deprotonated L2 ligands bind pal ladium (II) in a tetradentate (C,N,N,O) fashion whereas in the case of [(A)PdCl], the deprotonated A ligands bind Pd(II) in tridentate (C,N,N) manner. X ray structures of [(L1)Pd], (2a) and [(A1)PdCl] (4a) were determined to confirm the molecular structures. Both the complexes 4a and 5a exhibited catalytic activ ity toward Suzuki and Heck reactions. Conversion of [(A)PdCl] to its oxidized form upon ligand oxidation is reported.