A unique homochiral metal–organic framework has
been successfully synthesized by solvothermal reaction of an achiral
flexible V-shaped ligand and a nanosized π-electron-deficient
pyridine ligand based on cobalt(II) salt, [Co(L)(DPNDI)<sub>0.5</sub>]<sub><i>n</i></sub> (<b>1</b>) (H<sub>2</sub>L =
4,4′-dicarboxydiphenylamine, DPNDI = <i>N</i>,<i>N</i>′-di-(4-pyridyl)-1,4,5,8-naphthalenediimide); the
helixes assembled by H<sub>2</sub>L and cobalt(II) paddle-wheel centers
are left-handed and transform the framework to chiral. Also, the
inserting of the DPNDI transforms the original <b>dia</b> net
constructed by H<sub>2</sub>L and cobalt(II) paddle-wheel centers
to a 3-fold <b>jsm</b> net. This is the first example of interpenetrated <b>jsm</b> net. In addition, the chiral property of bulk products
is confirmed by circular dichroism spectra (CD), and the thermal stability
and the magnetic properties are also investigated