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Coordination-Driven Supramolecular Assembly of Phosphole-Based π-Conjugated Ligands

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Phosphorus Compounds

Part of the book series: Catalysis by Metal Complexes ((CMCO,volume 37))

Abstract

π-chromophores having a (2-pyridyl)phosphole moiety act as heteroditopic P,N-chelates towards a large range of transition metals. Due to the different nature of the donor atoms in these ligands, stereoselective coordination chemistry processes allow organizing of these derivatives into sophisticated architectures. Coordination-driven synthesis of C 2-symmetrical metallic complexes active in non-linear optics (NLO) and chiral metal-bis(azahelicene phosphole) assemblies are described. Furthermore, 1-phenyl-bis(2-pyridyl)phosphole can act as a N,P,N-chelate with bridging P-atoms in a very original coordination mode to stabilize a variety of metal dimers. Use of such Cu(I) dimers as molecular clips allows the characterization of π-stacked [2,2]metallacyclophanes that self-assemble in a very general way in the solid state along π-stacked columns.

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Crassous, J., Lescop, C., Réau, R. (2011). Coordination-Driven Supramolecular Assembly of Phosphole-Based π-Conjugated Ligands. In: Peruzzini, M., Gonsalvi, L. (eds) Phosphorus Compounds. Catalysis by Metal Complexes, vol 37. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-3817-3_11

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