The electrochemical character of bilirubin（BR）-M2+(M2+=Cd2+,Cu2+,Zn2+,Ca2+,Fe2+)Langmuir-Blodgett（LB）film modified glassy carbon electrode was investigated,and was compared with that of BR-LB film modified glassy carbon electrode and that of BR and M2+in solution.On BR-M2+-LB film modified glassy carbon electrodes,one anodic peak for BR-M2+ complex was observed at-679～-842mV,and the anodic peak potential of BR shifted towards to ositive from 453 mV to 477～493 mV.BR-M2+（in solution）formed BR-M2+ complex with BR on the BR-LB film modified glassy carbon electrode,at the same time,M2+permeated BR-LB film and occrred electrode reaction.The anodic peak potential of BR-M2+ complex on LB film shifted towards positive with the increasing of stability of biologic metal complex.In BR and M2+ solution,the potentials of two anodic peaks for BR（400 mV and 305 mV）was shifted positive 19～51 mV due to BR-M2+ complex forming,and this potential was effected by the ratio of BR and M2+.Moreover,a pair of symmetrical adsorption peak was appeared at nearly 0 mV,which indicated the hydrophobicity of this complex molecule was stronger than that of BR molecule.
A series of complexes were synthesized using piazselenole（NS） 5-methyl piazselenole（MB） and 4,5-benzopiazselenole（BS）as ligands and Cu2+ as cation in liquid-phase and solid-phase reaction.The complexes were characterized and compared by ICP-AES,EA,IR,UV-Vis,and XRD etc.The coordinating mechanism and the spectral properties are also discussed.
Under microwave radiation conditions,a series of heterocyclic aromatic selenium compounds of 2,1,3-benzoselena-diazole(BS);1,2,5-selenadiazolo[3.4-b]pyridine(SPb);5-methy1-2,1,3-benzo-[3,4-c]selenadiazole(MB);5,7-dihydroxy-1,2,5-selenadiazolo-[3,4-d]pyrimi dine(DHSP)and 2,1,3-naphtho-[2,3-c]selenadiazole(NS) were synthesized with their respective ortho-aromatic diamines and selenium dioxide,and their yields were between 29% and 84%.The products obtained from the microwave solid-state reactions were characterized by IR,XRD,UV,FS and EA.
