A new family of molecule-based magnets of general formula V[TCNQR(2)](2)(.)zCH(2)Cl(2) has been synthesized and characterized (TCNQ = 7,7,8,8-tetracyano-p-quinodimethane; R = H, Br, Me, Et, i-Pr, OMe, OEt, and OPh). In addition, solid solutions of V[TCNQ](x)[TCNQ(OEt)(2)](2-x)(.)zCH(2)Cl(2) composition have been prepared. Except R = Br, magnetic ordering was observed for all materials, with T-c values between 7.5 K (R = Me) and 106 K (R = OEt), with R = H at 52 K. The substitution of electron-donating OMe and OEt groups for H in TCNQ increased T-c, whereas the substitution of less electron-donating alkyl groups (with respect to alkoxy groups) decreased T-c. The results of MO calculations indicate that neither the spin nor charge densities of the disubstituted TCNQs are sufficiently different to explain the wide range of critical temperatures. Although the structures of the amorphous materials are not known, it is proposed that the oxygen atom of the [TCNQR(2)](.-) acceptor (R = OMe and OEt) and the V(II) interact to form a seven-membered ring. This interaction could stabilize the structure and enhance the magnetic coupling, leading to an increased T-c. The magnetic properties of V[TCNQ](x)[TCNQ(OEt)(2)](2-x)(.)zCH(2)Cl(2) deviated from the expected linear relationship with respect to x, exhibiting magnetic behavior more characteristic of a step function in a plot of T-c versus x.