A new mesogenic crosslinking agent M-1 was synthesized to minimize the perturbations of a nonmesogenic crosslinking agent for liquid crystalline elastomers. The synthesis of new side-chain liquid crystalline elastomers containing a rigid mesogenic crosslinking agent M-1 and a nematic monomer M-2 is described by a one-step hydrosilylation reaction. The chemical structures of the obtained monomers and elastomers were confirmed by H-1 NMR and FTIR spectroscopy. The mesomorphic properties and phase behavior were investigated by differential scanning calorimetry, polarizing optical microscopy, and X-ray diffraction measurements. The influence of the crosslinking units on the phase behavior is discussed. The elastomers containing less than 15 mol % of the crosslinking units showed elasticity, reversible phase transition, and nematic-threaded texture. However, when the crosslinking density reached 21.6 mol %, the mesophase of polymer P-8 disappears. The adoption of a mesogenic crosslinking agent diminishes the perturbation of a nonmesogenic crosslinking agent on mesophase of liquid crystalline elastomers, and isotropic temperature and a mesomorphic temperature range slightly decreased with increasing content of the crosslinking agent. In addition, X-ray analysis shows nematic polydomain network polymers can transform into smectic monodomain by stress induction, leading to the orientation formation macroscopically. (C) 2004 Wiley Periodicals, Inc.