A fluorene-based diphosphinite ligand, its Ni, Pd, Pt, Fe, Co and Zn complexes and the first structurally characterized diphosphinate metal chelates

作者：Li Changxiu; Pattacini Roberto; Braunstein Pierre^*

来源：Inorganica Chimica Acta, 2010, 363(15): 4337-4345.

DOI：10.1016/j.ica.2010.06.007

• Diphosphinites
• Diphosphinates
• Fluorene
• Anion coordination
• Host-guest
• Ligand conformation

The diphosphinite ligand 9,9-(Ph2POCH2)(2)-fluorene (1) was reacted with group 10 metal dichlorides to form chelate complexes of formula [MCl2(1)] (M=Ni, 2; M=Pd, 3; M=Pt, 4) showing 8-membered metallocycles. Chloride abstraction from 3 with AgOTf afforded the dinuclear complex [M(mu-Cl)Pd(1)](2)(OTf)(2) (5), in which the ligand adopts a different conformation with respect of 3. In 5, the fluorene moiety and the phenyl groups display stabilizing interactions with the anion which is located close to the metal centre. With Fe(II), Co(II) and Zn(II) chlorides, the non-isolated intermediates [MCl2(1)] readily undergo oxidation to [MCl2(1(ox))] (M=Fe, 6; M=Co, 7; M=Zn, 8; 1(ox) = 9,9-(Ph2P(O)OCH2)(2)-fluorene) in which the diphosphinate ligand and the metal centre form 10-membered metallocycles. Complexes 6-8 are the first examples of structurally characterized diphosphinate metal chelates. The Zn(II) diphosphinite complex [ZnCl2(1)] (9) could be observed by NMR spectroscopy, along with the mixed phosphinite-phosphinate, mono-oxidized complex which is an intermediate in the formation of 8. Complex [ZnCl2(9.9-fluorenedimethanol)(Ph2P(O)H)] (10) was also observed as hydrolysis product of 9. The X-ray molecular structures of 2, 3, 5.2OTf, 6, 7, 8 and 10 are reported.

• 出版日期2010-12-10