Abstract
The reaction of Co(NCS)(2) with N-methylaniline leads to the formation of [Co(NCS)(2)(N-methylaniline)(2)](n) (1), in which the cobalt(II) cations are octahedrally coordinated and linked into linear chains by pairs of thiocyanate anions. In contrast to [Co(NCS)(2)(aniline)(2)](n) (2) reported recently, in which the Co(NCS)(2) chains are linked by strong interchain N-H···S hydrogen bonding, such interactions are absent in 1. Computational studies reveal that the cobalt(II) ions in compound 1 show an easy-axis anisotropy that is lower than in 2, but with the direction of the easy axis being similar in both compounds. The high magnetic anisotropy is also confirmed by magnetic and FD-FT THz-EPR spectroscopy, which yield a consistent g(z) value. These investigations prove that the intrachain interactions in 1 are slightly higher than in 2. Magnetic measurements reveal that the critical temperature for magnetic ordering in 1 is significantly lower than in 2, which indicates that the elimination of the hydrogen bonds leads to a weakening of the interchain interactions. This is finally proven by FD-FT THz-EPR experiments, which show that the interchain interaction energy in the N-methylaniline compound 1 is nine-fold smaller than in the aniline compound 2.