Abstract

Two reactions are induced form pure solid methyl viologen dichloride, MV2+(Cl–)2, upon heating under vacuum: warming over 50 °C yields Cl–MV+˙Cl˙via an intracomplex electron-transfer process; warming to 180 °C yields 4,4′-bipyridine and CH3Cl, probably via a second intracomplex charge-transfer process. Both these reactions are also shown to occur upon visible excitation of dehydrated MV2+(Cl–)2. In this case, the MV2+→MV+˙ reduction does not arise from direct photochemistry but rather results from thermal activation. Similar treatment of the bromide and iodide salts, MV2+(Br–)2 and MV2+(I–)2, lead only to the dealkylation products. These reactions have been investigated and followed using i.r., Raman, u.v.-visible, and e.s.r. spectroscopy and their mechanisms are discussed.

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