The organometallic pseudo-polymorphism that arises from cocrystallisation o
f organometallic molecules or ions with solvent molecules is discussed, tog
ether with the possibility of interconversion between polymorphs and pseudo
-polymorphs. Three cases have been investigated: (i) the quantitative prepa
ration of a monohydrated pseudo-polymorph of the supramolecular salt [Co-II
I(eta (5)-C5H5)(2)](+)[Fe(eta (5)-C5H4CO2H)(eta (5)-C5H4CO2)](-) 1 by grind
ing the powder material and subsequently nucleating and crystallising the h
ydrated form [Co-III(eta (5)-C5H5)(2)](+)[Fe(eta (5)-C5H4CO2H)(eta (5)-C5H4
CO2)](-).H2O 2, (ii) the quantitative preparation, nucleation and crystalli
sation of the elusive anhydrous form of the neutral zwitterion [Co-III(eta
(5)-C5H4CO2H)(eta (5)-C5H4CO2)] 4 by thermal dehydration of the hydrated sp
ecies [Co-III(eta (5)-C5H4CO2H)(eta (5)-C5H4CO2)]. 3H(2)O 3, and (iii) the
formation of the salt [Ru-II(eta (6)-C6H6)(2)][BF4](2) 5 either by direct c
rystallisation from water or by desolvation of the pseudo-polymorph [Ru-II(
eta (6)-C6H6)(2)][BF4](2). MeNO2 6 obtained from nitromethane. In order to
investigate the processes, single crystal and powder X-ray diffraction meas
urements as well as thermogravimetry and differential scanning calorimetry
have been carried out. These results show, inter alia, how elusive polymorp
hic or pseudo-polymorphic modifications of a given substance can be obtaine
d by non-solution methods.