“…1.330 (3)/~ in Cu(PM-H)2.2H20, and 1.307 (4) and 1.314 (4)A in Cu(PM)2(NO3)E.H20; K. J. , and is closer to distances observed in compounds whose phenolic groups are un-ionized [1.343 (6) ,/~ in PN.HC1; Bacon & Plant, 1980]. It is particularly interesting that pyridoxine does coordinate to metals as the zwitterion (Mosset et al, 1978). The transformation to the zwitterion facilitates coordination by the phenolic group, and is reminiscent of the tautomeric change which occurs when pyridoxamine coordinates to metal ions (K. J.…”