A crystal-engineering approach to organic ferrimagnetics is reported. Coulo
mbic energy between cationic biradical with S=1 and anionic radical with S=
1/2 is a promising driving force of co-crystallizing the hetero-molecular a
ssemblage in a controllable manner. As a cationic component of "organic sal
t ferrimagnetics", two kinds of nitronyl nitroxide biradicals, 2,6- and 3,5
-substituted pyridine derivatives, were examined. It was predicted from sem
i-empirical molecular orbital calculations that both the 2,6- and 3,5-deriv
atives have the tripler ground states both in the neutral and cationic stat
es. The molecular ground state of the 2,6-biradical in the neutral state wa
s found to be triplet from the magnetic susceptibility measurement, while t
he susceptibility and ESR measurements suggested the singlet ground state f
or the 3,5-biradical. The potential of the pyridine-based biradicals as the
components of "organic salt ferrimagnetics" is discussed.