Crystallization and crystal structure analysis of chlorohydrates of either tri- or tetracationic copper porphyrins, namely copper(5,10,15-tris(N-methyl-pyridinium-4-yl)-20-pyridine-porphyrinato) (1) and copper(5,1 0,1 5,20-tetrakis (N-methyl-pyridinium-4-yl)-porphyrinato), respectively, have been performed. Two crystalline forms, 2 and 3, of the latter have been obtained under different preparation conditions. A novel kind of slipped stack chains of these cationic porphyrins has been detected. The pronounced saddle conformation of the porphyrin reveals T-like interactions between the peripheral pyrrole Cb-Cb "double bond" and the metal center. DFT calculations on the isolated porphyrins clearly show the HOMO orbitals with the correct topology to yield a bonding interaction among the stacked porphyrin units. To our knowledge, a slipped stack chain of positively charged porphyrins has never been previously reported, if the arrangement of faced units of monocationic metalloporphyrins or phthalocyanins is excluded.
|Titolo:||Assembly of positively charged porphyrins driven by metal ions: A novel polymeric arrangement of cationic metalloporphyrin|
|Data di pubblicazione:||2004|
|Appare nelle tipologie:||1.1 Articolo in rivista|
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|Inorg.Chem.2004.pdf||Versione Editoriale (PDF)||Non specificato||Administrator|