Synthesis, Characterization, and Properties of a Titanium(IV)-Tetrathiafulvalene-Based Complex

被引:1
作者
Casas, Jaison [1 ]
Baudron, Stephane A. [1 ]
Bonnefont, Antoine [2 ,3 ]
Chaumont, Alain [1 ]
Chauvin, Jerome [4 ]
Mobian, Pierre [1 ]
Ruhlmann, Laurent [2 ]
机构
[1] Univ Strasbourg, CNRS, CMC UMR 7140, F-67000 Strasbourg, France
[2] Universite? Strasbourg, CNRS, IC UMR 7177, F-67000 Strasbourg, France
[3] LEPMI, Univ Grenoble Alpes, Univ Savoie Mont Blanc, LEPMI,Grenoble INP, F-38000 Grenoble, France
[4] Univ Grenoble Alpes, CNRS, DCM UMR 5250, F-38000 Grenoble, France
关键词
TETRATHIAFULVALENE; DYAD; STATE; TIO2; EFFICIENT; SURFACES; VALENCE; WATER;
D O I
10.1021/acs.inorgchem.4c01389
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
To deeply investigate the interaction between a tetrathiafulvalene (TTF) unit and a Ti(IV) center, a monomeric heteroleptic octahedral Ti(IV) complex containing a diimine ligand composed of a 1,10-phenanthroline core fused with a TTF fragment (ligand 2a) was prepared. The stable complex formulated as Ti(1)(2)(2a), where 1 is a 2,2 '-biphenolato derivative, was efficiently synthesized by following a one-step approach. This complex and its model species [Ti(1)(2)(2b)] were fully characterized in solution, and their solid-state structures were established by single-crystal X-ray diffraction analysis. Density functional theory calculations allowed the assignment of the frontier orbitals involved in the electronic transitions characterized by ultraviolet-visible absorption spectroscopy. Electrochemical and spectroelectrochemical studies revealed that the TTF unit within Ti(1)(2)(2a) can undergo two reversible one-electron oxidation processes; a reversible one-electron reduction of the Ti(IV) atom was highlighted. The photophysical measurements performed for this donor-acceptor molecular system indicated that an electron transfer process upon light excitation occurred within Ti(1)(2)(2a).
引用
收藏
页码:10057 / 10067
页数:11
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