Ag(6)L(6)-type coordination nanotubular structures have been assembled from 6 Ag(I) ions and 6 T-shaped ligands, 4-(3,5-bis(diphenylphosphino)phenyl)pyridine; the nanotubes represent a discrete molecular architecture of a number of polymeric structures assembled from dimeric building blocks.

A catalytic system consisting of the ruthenium(II) complex [Ru(η³-2-C3H4Me)(CO)(dppf)][SbF6] (dppf=1,1'-bis(diphenylphosphino)ferrocene) and trifluoroacetic acid has been used to promote the coupling of secondary propargylic alcohols with 6-chloro-4-hydroxychromen-2-one. The reactions afforded unusual 2-methylene-2,3-dihydrofuro[3,2-c]chromen-2-ones in good yields.

Iron nanoparticles, either formed in situ stabilized by 1,6-bis(diphenylphosphino)hexane or polyethylene glycol (PEG), or preformed stabilized by PEG, are excellent catalysts for the cross-coupling of aryl Grignard reagents with primary and secondary alkyl halides bearing beta-hydrogens and they also prove effective in a tandem cyclization/cross-coupling reaction.

A catalytic amount of 1,2-bis(diphenylphosphino)benzene (DPPBz) achieves selective cleavage of sp(3)-carbon-halogen bond in the iron-catalysed cross-coupling between polyfluorinated arylzinc reagents and alkyl halides, which was unachievable with a stoichiometric modifier such as TMEDA; the selective iron-catalysed fluoroaromatic coupling provides easy and practical access to polyfluorinated ar...

Much effort has been devoted to the development of efficient asymmetric synthetic methods for the preparation of enantiomerically enriched compounds.1,2 Among various methods for the enantiomerically selective synthesis of chiral organic compounds from prochiral precursors, enantioselective catalytic hydrogenation of dehydro precursors has been extensively developed.3 In fact, asymmetric hydrog...

Two self-assembled redox-active cages are presented. They are obtained by coordination-driven self-assembly of a tetra-pyridile tetrathiafulvalene ligand with cis-M(dppf)(OTf)₂ (M = Pd or Pt; dppf = 1,1'-bis(diphenylphosphino)ferrocene; OTf = trifluoromethane-sulfonate) complexes. Both species are fully characterized and are constituted of 12 electro-active subunits that can be reversibly oxidi...

N-Diphenylphosphino-7-aza-benzobicyclo[2.2.1]hept-2-ene (2) behaves as a chelating phosphine-alkene ligand for Pd(0) and Pd(II), promoting direct alkyl-alkyl and indirect alkyl-halide reductive elimination reactions due to the stabilisation of the resulting bis(phosphine-alkene)Pd(0) complex.

A series of homoleptic and heteroleptic platinum(II) complexes [Pt(C[triple bond]CFc)2(L-L)] (L-L = COD 1, 1,1'-bis(diphenylphosphino)ferrocene (dppf) 2), Q2[cis/trans-Pt(C6F5)2(C[triple bond]CFc)2] (cis, Q = PMePh3, 3; trans, Q = NBu4, 4), (NBu4)[Pt(bzq)(C[triple bond]CFc)2] 5 (Hbzq = 7,8-benzoquinoline) and (NBu4)2[Pt(C[triple bond]CFc)4] 6 has been synthesized and characterized spectroscopic...

catalytic amount of ce(iv) as ceric triethylammonium nitrate (ctean) in dichloromethane or acetone can bring about an efficient tetrahydropyranylation of different types of alcohols to afford the corrsesponding tetrahydropyranyl ethers in high yields. deportection of tetrahydropyranyl ethers can also be achieved efficiently in the presence of this catalyst in methanol.