Ethynyl porphyrins bridging bis(phosphine)platinum(II) centers: molecular models for conjugated organometallic porphyrin polymers

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Angelica Ferri, Giovanni Polzonetti, Silvia Licoccia, Roberto Paolesse, Donata Favretto, Piero Traldi and Maria V. Russo


Abstract

Linear ethynylporphyrin-bridged platinum(II) complexes, [X(R3P)2Pt–C[triple bond, length half m-dash]C–Zn(por)–C[triple bond, length half m-dash]C–Pt(PR3)2Y] [Zn(por) is a non-ethynylated porphyrin 1a] and related oligomers have been synthesized. Di- and tri-nuclear platinum centers are linked to different porphyrin arrays; the end groups Pt(PR3)2X and Pt(PR3)2Y (R = n-Bu or Ph; X = Y = Cl or I; X = Cl, Y = I) show that a ligand exchange Cl → I also occurs. The compounds containing PBu3 as the ligand are more stable than the corresponding PPh3 ones. The dinuclear platinum dimers containing one bridging porphyrin have been isolated and characterized by IR, UV/VIS, 1H NMR and MALDI (matrix assisted laser desorption/ionization) mass spectroscopies. The mixture of longer oligomers was separated from the crude reaction products and could be identified by MALDI. The cis–trans isomerization of the porphyrin complexes with respect to the platinum precursor complexes, i.e. trans-[PtCl2(PBu3)2], cis-[PtCl2(PPh3)2] and trans-[PtH(Cl)(PPh3)2], was observed. The dimers and oligomers are expected to be model molecules for long chain organometallic polymers.


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