Keto-acid chloride and diketone intermediates in the acylation of ferrocene by arylene bis-acid chlorides.: Crystal and molecular structure of 4-ferrocenylcarbonyl-4′-chlorocarbonylbiphenyl:: intermolecular association by means of strong C-H•••O hydrogen bonds and π••• π stacking interactions

Acylation of ferrocene with arylene bis-acid chlorides yields deep-red polymeric products. However, under controlled conditions two types of intermediate can be isolated and characterised: the keto-acid chlorides FcCO(arylene)COCl 1 [Fc = (C5H5)Fe(C5H4); a arylene = 4,4'-C6H4C6H4, b arylene = 1,3-C6H4, c arylene = 1,4-C6H4], followed in the case of 1a and 1b by the diketones FcCO(arylene)COFc 2a and 2b, although no conversion of 1c to 2c occurs. Similarly, use of 1,3,5-benzenetricarbonyl trichloride yielded 1,3,5-C6H3(COFc)(3). In the crystal structure of 1a, there are four independent molecules: pairs of molecules are linked into dimers by strong C-H ... O hydrogen bonds, and these dimers are linked into chains by pi...pi stacking interactions. (C) 1999 Elsevier Science S.A. All rights reserved.