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Structural Insight into Order-Disorder Transition and Charge-Transfer Phase Transition in an Iron Mixed-Valence Complex (n-C3H7)4N[FeIIFeIII(dto)3] with a Two-Dimensional Honeycomb Network
被引:10
作者:
Itoi, Miho
[1
]
Okazawa, Atsushi
[2
]
Yamaura, Jun-ichi
[3
]
Maki, Sachiko
[3
]
Komatsu, Tokutaro
[4
]
Maurin, Isabelle
[5
]
Codjovi, Epiphane
[6
]
Boukheddaden, Kamel
[6
]
Kojima, Norimichi
[7
]
机构:
[1] Nihon Univ, Sch Med, Inst Liberal Educ, Div Phys,Itabashi Ku, Tokyo 1738610, Japan
[2] Univ Tokyo, Grad Sch Arts & Sci, Dept Basic Sci, Meguro Ku, Tokyo 1538902, Japan
[3] Tokyo Inst Technol, Mat Res Ctr Element Strategy, Yokohama, Kanagawa 2268503, Japan
[4] Nihon Univ, Sch Med, Inst Liberal Educ, Div Chem,Itabashi Ku, Tokyo 1738610, Japan
[5] Univ Paris Saclay, CNRS, Ecole Polytech, Phys Matiere Condensee, Route Saclay, F-91120 Palaiseau, France
[6] Univ Versailles St Quentin En Yvelines, CNRS, UMR 7643, Grp Etud Matiere Condensee, 45 Ave Etats Unis, FR-78035 Versailles, France
[7] Toyota Phys & Chem Res Inst, Nagakute, Aichi 4801192, Japan
关键词:
POROUS COORDINATION POLYMERS;
SLOW MAGNETIC-RELAXATION;
THERMAL-EXPANSION;
CRYSTAL-STRUCTURE;
SPIN TRANSITION;
HEAT-CAPACITY;
M-II;
SERIES;
FE;
CO;
D O I:
10.1021/acs.inorgchem.8b02211
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
The structural properties of the iron mixed valence complex (n-C3H7)(4)N[(FeFeIII)-Fe-II(dto)(3)] (dto = dithiooxalato, C2O2S2) have been investigated by single-crystal X-ray diffraction (SCXRD) at low temperatures. (n-C3H7)(4)N-[(FeFeIII)-Fe-II(dto)(3)] has two-dimensional (2D) honeycomb layers consisting of alternating Fe-II and Fe-III arrays bonded by bisbidentate dithiooxalato ligands. Upon cooling, a superlattice structure with q = (1/3, 1/3, 0) was observed below 260 K, which corresponds to an order disorder transition of the (n-C3H7)(4)N+ ions between the honeycomb layers. The charge transfer phase transition (CTPT) occurs at T-C up arrow 1/2 similar to 120 K and T-C down arrow 1/2 similar to 90 K upon heating and cooling, respectively, with an electron transfer between the Fe-II and Fe-III ions, accompanied by a spin-state change, Fe-II (S = 2; HS)-O2C2S2-Fe-III (S = 1/2; LS) <-> Fe-III (S = 5/2; HS)-O2C2S2-Fe-II (S = 0; LS). During the CTPT, the intersheet [(FeFeIII)-Fe-II(dto)(3)] distance decreased monotonously upon cooling, and an abrupt structural contraction was observed in the hexagonal 2D network. The volume contraction during the CTPT was quite small (similar to 0.7%), and differences in the structural distortions at the FeS6 and FeO6 sites were not found in the vicinity of the CTPT. We also calculated the orbital energies and the occupied spin states for the [Fe(O2C2S2)(3)] and [Fe(S2C2O2)(3)] octahedra in the vicinity of the CTPT by density functional theory (DFT). Because the local symmetry around the two coordinating iron ions is already lowered to trigonal symmetry, the CTPT did not cause any further deformation. This symmetry invariance resulted in an absence of orbital contributions to the total entropy change (Delta S) in the CTPT, which is in agreement with the previous heat capacity measurements. [Nakamoto, T; Miyazaki, Y; Itoi, M; Ono, Y; Kojima, N; Sorai, M. Heat Capacity of the Mixed-Valence Complex {[(n-C3H7)(4)N][(FeFeIII)-Fe-II(dto)(3)]}(infinity), Phase Transition because of Electron Transfer, and a Change in Spin-State of the Whole System.
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页码:13728 / 13738
页数:11
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