2014
DOI: 10.1016/j.jorganchem.2014.01.008
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Comparison of coordination mode of some biphosphine ligands in cyclometalated organoplatinum(II) complexes

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Cited by 13 publications
(4 citation statements)
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“…6 In this context, some of various C^N cycloplatinated(II) complexes with aryl ligands (p-tolyl, p-anisole, phenyl) and their reactions have been reported in the literature. [7][8][9][10][11][12] To the best of our knowledge, the presence of aryl groups as ancillary ligands in the rollover cycloplatinated(II) complexes is very scarce in the published resources. 13 In this way, thermal rearrangement of the complex [Pt(bpy)(Ar)2] (bpy = 2,2´-bipyridine, Ar = C6H5, p-t Bu-C6H4 and p-CF3-C6H4) results in the formation of three-coordinated monoaryl [Pt(C^N)(Ar)] intermediates via rollover cycloplatination process.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…6 In this context, some of various C^N cycloplatinated(II) complexes with aryl ligands (p-tolyl, p-anisole, phenyl) and their reactions have been reported in the literature. [7][8][9][10][11][12] To the best of our knowledge, the presence of aryl groups as ancillary ligands in the rollover cycloplatinated(II) complexes is very scarce in the published resources. 13 In this way, thermal rearrangement of the complex [Pt(bpy)(Ar)2] (bpy = 2,2´-bipyridine, Ar = C6H5, p-t Bu-C6H4 and p-CF3-C6H4) results in the formation of three-coordinated monoaryl [Pt(C^N)(Ar)] intermediates via rollover cycloplatination process.…”
Section: Introductionmentioning
confidence: 99%
“…Figure 1 shows three different possible modes of binding for diphosphines in cycloplatinated(II) complexes. 8,9,11,[33][34][35][36][37][38][39][40][41][42][43][44] Figure 1. Different binding modes for diphosphine ligands in cycloplatinated(II) complexes.…”
Section: Introductionmentioning
confidence: 99%
“…2 A similar bond cleavage reaction has been observed in analogues cycloplatinated(II) complexes. 6,10,31,[39][40][41] Complexes 1 and 2 are air-stable and obtained in high yields. They are soluble in halogenated solvents such as CH2Cl2 or CHCl3 and stable for several days at room temperature in the solution.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
“…Bidentate ligands with their steric hindrance reduces the transfer of negative charge on Pt (II) central metal and stabilizes this center toward oxidation reaction . Oxidative addition of various reagents, including alkyl and allyl halides to organoplatinum (II) complexes bearing diimine ligands such as bipy (2,2′‐bipyridine) and phen (1,10‐phenanthroline) leads to fabrication of organoplatinum (IV) complexes . Kinetic studies of colorful diimine Pt (II) complexes are facile due to characteristic sharp metal‐to‐ligand charge transfer (MLCT) bands in the visible region .…”
Section: Introductionmentioning
confidence: 99%