Photochemical Formation of Ferrimagnetic Chains from a Pair of Polymeric Complexes Made of Octahedral Bis(hexafluoroacetylacetonato)manganese(II) with Diazodi(4-pyridyl)methane in the Cis and Trans Configurations as Repeating Units

Two kinds of 1:1 manganese complexes a and b of bis(hexafluoroacetylacetonato)manganese(II) coordinated with diazodi(4-pyridyl)methane ( 1 ) were prepared. Complexes a and b crystallize in the orthorhombic space group Pbca and in monoclinic C 2/ c, respectively. Two pyridyl nitrogen atoms from two different molecules of 1 are coordinated in the cis and trans configurations to the manganese ion to form helical and zigzag infinite chains of octahedral manganese complexes in complexes a and b, respectively. The magnetic susceptibilities (χ mol ) of both crystals before and after irradiation were measured on a SQUID susceptometer and revealed χ mol T vs T plots characteristic of ferrimagnetic chains after irradiation for 97 h; interaction between the manganese(II) ion and the photogenerated carbene is antiferromagnetic in both complexes. The antiferromagnetic exchange coupling parameters ( J ) in the photolyzate of complex a and b were estimated by a theoretical treatment through a procedure of extrapolation by using small rings to be J / k B = −34.8 ± 0.8 and −24.4 ± 0.5 K, respectively. Maximum χ mol T values of 210 at 5 K for cis- and 246 emu·K·mol - 1 at 1.9 K for trans complexes correspond to correlation lengths of 186 and 218 manganese−carbene S = 3 / 2 units, respectively.