Two new layered bimetallic sulfides: Solvothermal synthesis, crystal structure, optical and magnetic properties

被引:22
作者
Lin, Zhien [1 ]
Bu, Xianhui [2 ]
Feng, Pingyun [3 ]
机构
[1] Sichuan Univ, Coll Chem, Chengdu 610064, Peoples R China
[2] Calif State Univ Long Beach, Dept Chem & Biochem, Long Beach, CA 90840 USA
[3] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
关键词
Solvothermal synthesis; Layered structure; Bimetallic sulfide; Optical property; Magnetic property; OPEN-FRAMEWORK CHALCOGENIDES; ANTIMONY SULFIDE; MN-2(L)SB2S5 FAMILY; BUILDING UNITS; CHEMISTRY; CLUSTERS; CHANNELS; THIOANTIMONATES(III); ALUMINOPHOSPHATE; TRANSITION;
D O I
10.1016/j.micromeso.2010.03.010
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two new bimetallic sulfides, (Haep)(2)center dot Ga(2)Sb(2)S(7) (1) and Mn(2)(phen)Sb(2)S(5) (2), have been synthesized under solvothermal conditions, where aep = 1-(2-aminoethyl)piperazine and phen = 1,10-phenanthroline. The structure of 1 consists of GaS(4) tetrahedra and SbS(3) trigonal pyramids and has a layered structure with 8-membered-ring windows. Interestingly, the interlayer organic cations form helices through extensive hydrogen bonds. Compound 2 has a neutral layered structure containing infinite Mn-S sheets. The organic species are attached directly to Mn atoms within the layers by covalent bonds and protrude into the interlayer region. Both compounds 1 and 2 exhibit intense photoluminescence upon photoexcitation at 360 nm. Magnetic susceptibility measurements demonstrate the existence of antiferromagnetic interactions in compound 2. Crystal data: 1, orthorhombic, P2(1)2(1)2(1) (No. 19), a = 9.9274(2) angstrom, b = 12.9201(3) angstrom, c = 21.2254(4) angstrom, V = 2722.43(10) angstrom(3), Z = 4; 2, monoclinic, P2(1)/c (No. 14), a = 12.6385(3)angstrom, b = 12.3998 (3) angstrom, c = 12.3670(3) angstrom, beta = 111.8240(10)degrees, V= 1799.19(7) angstrom(3), Z 4. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:328 / 334
页数:7
相关论文
共 41 条
[1]   NANOPOROUS TIN(IV) CHALCOGENIDES - FLEXIBLE OPEN-FRAMEWORK NANOMATERIALS FOR CHEMICAL SENSING [J].
AHARI, H ;
BOWES, CL ;
JIANG, T ;
LOUGH, A ;
OZIN, GA ;
BEDARD, FL ;
PETROV, S ;
YOUNG, D .
ADVANCED MATERIALS, 1995, 7 (04) :375-378
[2]  
Bedard R., 1989, US Pat, Patent No. 4880761
[3]  
Bensch W, 1996, EUR J SOL STATE INOR, V33, P1149
[4]   Ortho-chalcogenostannates as ligands:: Syntheses, crystal structures, electronic properties, and magnetism of novel compounds containing ternary anionic substructures [M4(μ4-Se)(SnSe4)4]10- (M = Mn, Zn, Cd, Hg), ∞3[Hg4(μ4Se)(SnSe4)3]6-}, or ∞1{[HgSnSe4]2-} [J].
Brandmayer, MK ;
Clérac, R ;
Weigend, F ;
Dehnen, S .
CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (20) :5147-5157
[5]   Tetrahedral chalcogenide clusters and open frameworks [J].
Bu, XH ;
Zheng, NF ;
Feng, PY .
CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (14) :3356-3362
[6]  
Cheetham AK, 1999, ANGEW CHEM INT EDIT, V38, P3268, DOI 10.1002/(SICI)1521-3773(19991115)38:22<3268::AID-ANIE3268>3.0.CO
[7]  
2-U
[8]   From microporous to mesoporous molecular sieve materials and their use in catalysis [J].
Corma, A .
CHEMICAL REVIEWS, 1997, 97 (06) :2373-2419
[9]   Ordered porous materials for emerging applications [J].
Davis, ME .
NATURE, 2002, 417 (6891) :813-821
[10]   A coordination chemistry approach towards ternary M/14/16 anions [J].
Dehnen, Stefanie ;
Melullis, Maike .
COORDINATION CHEMISTRY REVIEWS, 2007, 251 (9-10) :1259-1280