Magnetic and optical studies on an S=6 ground-state cluster [Cr12O9(OH)3(O2CCMe3)15]:: Determination of, and the relationship between, single-ion and cluster spin Hamiltonian parameters

被引:45
作者
Collison, D
Murrie, M
Oganesyan, VS
Piligkos, S
Poolton, NRJ
Rajaraman, G
Smith, GM
Thomson, AJ
Timko, GA
Wernsdorfer, W
Winpenny, REP
McInnes, EJL
机构
[1] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England
[2] Univ Bern, Dept Biochem & Chem, CH-3000 Bern 9, Switzerland
[3] Univ E Anglia, Sch Chem Sci, Norwich NR4 7TJ, Norfolk, England
[4] Univ St Andrews, Sch Phys & Astron, St Andrews KY16 9SS, Fife, Scotland
[5] Moldavian Acad Sci, Inst Chem, MD-2028 Kishinev, Moldova
[6] CNRS, Lab Magnetisme Louis Neel, F-38042 Grenoble, France
关键词
D O I
10.1021/ic034541b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The dodecametallic Cr(III) cluster [Cr12O9(OH)(3)(O2CCMe3)(15)] has a ground spin state of S = 6 characterized by the spin Hamiltonian parameters g(ZZ) = 1.965, g(XX) = g(YY) = 1.960, D-S=6 = +0.088 cm(-1), and E-S=6 = 0 (where D and E are the axial and rhombic zero-field splitting parameters, respectively) as determined by multifrequency EPR spectroscopy and magnetization studies. Micro-SQUID magnetization studies reveal steps due to the fine structure of the ground state, with the spacing between the steps in excellent agreement with the D-S=6 value determined by EPR. Analysis of high-resolution optical data (MCD) allows us to determine the single-ion g values and D value (= -1.035 cm(-1)) of the constituent Cr(III) ions directly. A vector coupling analysis demonstrates that the cluster ZFS is almost entirely due to the single-ion component. Thus, the relative orientations of the local and cluster magnetic axes can lead to a cluster ZFS of opposite sign to the single-ion value, even when this is the only significant contribution.
引用
收藏
页码:5293 / 5303
页数:11
相关论文
共 51 条
[1]  
Abbati GL, 2001, CHEM-EUR J, V7, P1796, DOI 10.1002/1521-3765(20010417)7:8<1796::AID-CHEM17960>3.0.CO
[2]  
2-Y
[3]  
Abragam A., 1970, ELECT PARAMAGNETIC R, P430
[4]   ELECTRON-PARAMAGNETIC RESONANCE OF CHROMIUM(III) COMPLEXES OF TYPE-CIS-[CR(2,2'-BPY)2XY]Z, CIS-[CR(1,10-PHEN)2XY]Z, AND CIS-[CR(OX)2XY]Z IN FROZEN SOLUTIONS AND POWDERS [J].
ANDRIESSEN, WTM ;
GROENEWEGE, MP .
INORGANIC CHEMISTRY, 1976, 15 (03) :621-626
[5]   Single-molecule magnets:: Jahn-Teller isomerism and the origin of two magnetization relaxation processes in Mn12 complexes [J].
Aubin, SMJ ;
Sun, ZM ;
Eppley, HJ ;
Rumberger, EM ;
Guzei, IA ;
Folting, K ;
Gantzel, PK ;
Rheingold, AL ;
Christou, G ;
Hendrickson, DN .
INORGANIC CHEMISTRY, 2001, 40 (09) :2127-2146
[6]   Single molecule magnets:: High frequency electron paramagnetic resonance study of two isomeric forms of an Mn12 molecule [J].
Aubin, SMJ ;
Sun, Z ;
Rumberger, EM ;
Hendrickson, DN ;
Christou, G .
JOURNAL OF APPLIED PHYSICS, 2002, 91 (10) :7158-7160
[7]   Electronic structure of manganese(III) compounds from high-frequency EPR spectra [J].
Barra, AL ;
Gatteschi, D ;
Sessoli, R ;
Abbati, GL ;
Cornia, A ;
Fabretti, AC ;
Uytterhoeven, MG .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1997, 36 (21) :2329-2331
[8]   High-frequency EPR spectroscopy of large metal ion clusters: From zero field splitting to quantum tunneling of the magnetization [J].
Barra, AL ;
Brunel, LC ;
Gatteschi, D ;
Pardi, L ;
Sessoli, R .
ACCOUNTS OF CHEMICAL RESEARCH, 1998, 31 (08) :460-466
[9]   High-frequency EPR spectra of a molecular nanomagnet: Understanding quantum tunneling of the magnetization [J].
Barra, AL ;
Gatteschi, D ;
Sessoli, R .
PHYSICAL REVIEW B, 1997, 56 (13) :8192-8198
[10]  
Barra AL, 2000, CHEM-EUR J, V6, P1608, DOI 10.1002/(SICI)1521-3765(20000502)6:9<1608::AID-CHEM1608>3.3.CO