Cyclic iron tetra N-heterocyclic carbenes: synthesis, properties, reactivity, and catalysis

被引:22
作者
Schlachta, Tim P. P.
Kuehn, Fritz E. E. [1 ]
机构
[1] Tech Univ Munich, Sch Nat Sci, Dept Chem, Lichtenbergstr 4, D-85748 Garching, Germany
关键词
H BOND ACTIVATION; NONHEME IRON; ELECTRONIC-STRUCTURE; OLEFIN EPOXIDATION; CIS-DIHYDROXYLATION; MOLECULAR CATALYSIS; OXIDATION REACTIONS; 2-STATE REACTIVITY; HYDROGEN-PEROXIDE; EQUATORIAL LIGAND;
D O I
10.1039/d2cs01064j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclic iron tetracarbenes are an emerging class of macrocyclic iron N-heterocyclic carbene (NHC) complexes. They can be considered as an organometallic compound class inspired by their heme analogs, however, their electronic properties differ, e.g. due to the very strong sigma-donation of the four combined NHCs in equatorial coordination. The ligand framework of iron tetracarbenes can be readily modified, allowing fine-tuning of the structural and electronic properties of the complexes. The properties of iron tetracarbene complexes are discussed quantitatively and correlations are established. The electronic nature of the tetracarbene ligand allows the isolation of uncommon iron(iii) and iron(iv) species and reveals a unique reactivity. Iron tetracarbenes are successfully applied in C-H activation, CO2 reduction, aziridination and epoxidation catalysis and mechanisms as well as decomposition pathways are described. This review will help researchers evaluate the structural and electronic properties of their complexes and target their catalyst properties through ligand design.
引用
收藏
页码:2238 / 2277
页数:40
相关论文
共 274 条
[31]  
Chen K, 1999, ANGEW CHEM INT EDIT, V38, P2227, DOI 10.1002/(SICI)1521-3773(19990802)38:15<2227::AID-ANIE2227>3.0.CO
[32]  
2-B
[33]   Olefin cis-dihydroxylation versus epoxidation by non-heme iron catalysts:: Two faces of an FeIII-OOH coin [J].
Chen, K ;
Costas, M ;
Kim, JH ;
Tipton, AK ;
Que, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (12) :3026-3035
[34]   A predictably selective aliphatic C-H oxidation reaction for complex molecule synthesis [J].
Chen, Mark S. ;
White, M. Christina .
SCIENCE, 2007, 318 (5851) :783-787
[35]   Iron porphyrin-catalyzed olefination of carbonyl compounds with ethyl diazoacetate [J].
Cheng, GL ;
Mirafzal, GA ;
Woo, LK .
ORGANOMETALLICS, 2003, 22 (07) :1468-1474
[36]   High-Oxidation-State 3d Metal (Ti-Cu) Complexes with N-Heterocyclic Carbene Ligation [J].
Cheng, Jun ;
Wang, Lijun ;
Wang, Peng ;
Deng, Liang .
CHEMICAL REVIEWS, 2018, 118 (19) :9930-9987
[37]   Chloride binding by a polyimidazolium macrocycle detected via fluorescence, NMR, and X-ray crystallography [J].
Chi-Linh Do-Thanh ;
Khanal, Neelam ;
Lu, Zheng ;
Cramer, S. Alan ;
Jenkins, David M. ;
Best, Michael D. .
TETRAHEDRON, 2012, 68 (06) :1669-1673
[38]   Facile Nitrite Reduction and Conversion Cycle of {Fe(NO)}6/7 Species: Chemistry of Iron N-Confused Porphyrin Complexes via Protonation/Deprotonation [J].
Ching, Wei-Min ;
Chuang, Chuan-Hung ;
Wu, Chih-Wei ;
Peng, Chih-Hsiung ;
Hung, Chen-Hsiung .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (23) :7952-+
[39]   Calix[n]triazolium based turn-on fluorescent sensing ensemble for selective adenosine monophosphate (AMP) detection [J].
Cho, Jihee ;
Shin, Jinwoo ;
Kang, Minjung ;
Verwilst, Peter ;
Lim, Changhyun ;
Yoo, Hanbin ;
Kim, Jeung Gon ;
Zhang, Xingcai ;
Hong, Chang Seop ;
Kim, Jong Seung ;
Kim, Sanghee .
CHEMICAL COMMUNICATIONS, 2021, 57 (91) :12139-12142
[40]   ELECTROCHEMICAL AND SPECTROSCOPIC STUDIES OF IRON PORPHYRIN NITROSYLS AND THEIR REDUCTION PRODUCTS [J].
CHOI, IK ;
LIU, YM ;
FENG, D ;
PAENG, KJ ;
RYAN, MD .
INORGANIC CHEMISTRY, 1991, 30 (08) :1832-1839