摘要
The reaction of bis（1,2,4-triazolyl-4-yl） （btr） and MnClO4-6H20 gave rise to a Mn（II） complex comprised of unprecedented dinuclear Mn（II） units, {[Mn2（btr）s（H20）5]- （ClO4）4（H20）2]n （1）. Single-crystal X-ray diffraction analysis revealed that 1 crystallizes in the monoclinic space group C2/c. btr adopts two types of bridging modes. One serves as μ-N1 ：N2 bridge through one triazolyl ring of btr forming a dinuclear Mn（II） unit, and the other adopts an exo-bidentate mode using two nitrogen atoms from each triazolyl ring and links the dinuclear units into a 2D cationic layer. ClO4 acts as a counter anion and does not take part in coordination. Interestingly, 2D layers are packed in an ABCABC mode. ClO4- and uncoordinated water molecules locate between the adjacent layers, and extensive hydrogen bonds further stabilize the whole framework.
The reaction of bis（1,2,4-triazolyl-4-yl） （btr） and MnClO4-6H20 gave rise to a Mn（II） complex comprised of unprecedented dinuclear Mn（II） units, {[Mn2（btr）s（H20）5]- （ClO4）4（H20）2]n （1）. Single-crystal X-ray diffraction analysis revealed that 1 crystallizes in the monoclinic space group C2/c. btr adopts two types of bridging modes. One serves as μ-N1 ：N2 bridge through one triazolyl ring of btr forming a dinuclear Mn（II） unit, and the other adopts an exo-bidentate mode using two nitrogen atoms from each triazolyl ring and links the dinuclear units into a 2D cationic layer. ClO4 acts as a counter anion and does not take part in coordination. Interestingly, 2D layers are packed in an ABCABC mode. ClO4- and uncoordinated water molecules locate between the adjacent layers, and extensive hydrogen bonds further stabilize the whole framework.
基金
supported by NSFC(20971122)and SRF for ROCS,SEM
