13C NMR and relaxation studies of the nanomagnet Mn12-acetate -: art. no. 064420

被引:28
作者
Achey, RM [1 ]
Kuhns, PL
Reyes, AP
Moulton, WG
Dalal, NS
机构
[1] Florida State Univ, Dept Chem, Tallahassee, FL 32306 USA
[2] Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[3] Florida State Univ, Dept Phys, Tallahassee, FL 32306 USA
关键词
D O I
10.1103/PhysRevB.64.064420
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The nanomagnet [Mn12O12(CH3COO)(16)(H2O)(4)]. 2CH(3)COOH . 4H(2)O, also known as Mn-12, has been synthesized with C-13 labeling at the CH3 groups, and investigated by C-13 NMR at fields up to 23 T. Using oriented samples, it is possible to resolve four distinct 13C peaks at room temperature, located on both sides of the unshifted Larmor frequency. These peaks were assigned to the four hyperfine-shifted, magnetically inequivalent sets of (CH3)-C-13 groups in the Mn-12 lattice, based on a comparison with the crystal structure and point-dipole and spin-density calculations. These results establish that the unpaired electron spin density of the S = 10 system in this cluster extends over the entire molecular framework, not just the core. These results are discussed in relationship to inelastic neutron scattering measurements. The temperature and field dependence of the C-13 nuclear-spin-lattice-relaxation time T-1 on the least shifted peak was measured. A single weakly field-dependent minimum at about 60 K is observed in the temperature dependence of the measured T-1. The relaxation mechanism responsible for the T-1 minimum is ascribed mainly to hindered rotation of the methyl group of the acetate ligand at higher temperature, and to electronic spin fluctuations at lower temperature.
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共 41 条
[1]   Deuteron spin-lattice relaxation in the Mn12O12-acetate magnetic cluster [J].
Arcon, D ;
Dolinsek, J ;
Apih, T ;
Blinc, R ;
Dalal, NS ;
Achey, RM .
PHYSICAL REVIEW B, 1998, 58 (06) :R2941-R2943
[2]   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
[3]   SOLID-STATE PROTON SPIN RELAXATION AND METHYL AND T-BUTYL REORIENTATION [J].
BECKMANN, PA ;
ALHALLAQ, HA ;
FRY, AM ;
PLOFKER, AL ;
ROE, BA ;
WEISS, JA .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (01) :752-753
[4]   Excited-state X-band EPR in a molecular cluster nanomagnet -: art. no. 212401 [J].
Blinc, R ;
Cevc, P ;
Arcon, D ;
Dalal, NS ;
Achey, RM .
PHYSICAL REVIEW B, 2001, 63 (21)
[5]   RELAXATION EFFECTS IN NUCLEAR MAGNETIC RESONANCE ABSORPTION [J].
BLOEMBERGEN, N ;
PURCELL, EM ;
POUND, RV .
PHYSICAL REVIEW, 1948, 73 (07) :679-712
[6]   TEMPERATURE-DEPENDENCE OF METHYL REORIENTATION AT INTERMEDIATE HINDERING POTENTIALS [J].
BUEKENHOUDT, A ;
VANGERVEN, L .
PHYSICAL REVIEW B, 1992, 46 (09) :5377-5386
[7]   ALTERNATING-CURRENT SUSCEPTIBILITY, HIGH-FIELD MAGNETIZATION, AND MILLIMETER BAND EPR EVIDENCE FOR A GROUND S = 10 STATE IN [MN12O12(CH3COO)16(H2O)4].2CH3COOH.4H2O [J].
CANESCHI, A ;
GATTESCHI, D ;
SESSOLI, R ;
BARRA, AL ;
BRUNEL, LC ;
GUILLOT, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (15) :5873-5874
[8]   TIME DECAY OF THE REMANENT MAGNETIZATION IN SPIN-GLASSES [J].
CHAMBERLIN, RV ;
MOZURKEWICH, G ;
ORBACH, R .
PHYSICAL REVIEW LETTERS, 1984, 52 (10) :867-870
[9]  
Chudnovsky E. M., 1998, Macroscopic Quantum Tunneling of the Magnetic Moment
[10]   First- and second-order transitions between quantum and classical regimes for the escape rate of a spin system [J].
Chudnovsky, EM ;
Garanin, DA .
PHYSICAL REVIEW LETTERS, 1997, 79 (22) :4469-4472