Synthesis of Heterocyclic [8]Circulenes and Related Structures

被引:85
作者
Hensel, Thomas [1 ]
Andersen, Nicolaj N. [1 ]
Plesner, Malene [1 ]
Pittelkow, Michael [1 ]
机构
[1] Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen O, Denmark
关键词
circulenes; heterocycles; aromaticity; antiaromatcity; synthesis; geometry; cyclooctatetraenes; nucleus-independent shifts; DENSITY-FUNCTIONAL THEORY; POST-HARTREE-FOCK; CYCLO-OLIGOMERIZATION; CONDENSATION PRODUCTS; COMPLEX OXIDATION; PLANAR CYCLOOCTATETRAENE; STRONG ACIDS; COORDINATION POLYMERS; EFFICIENT SYNTHESIS; AROMATIC-COMPOUNDS;
D O I
10.1055/s-0035-1560524
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this account we give an overview of the synthesis and properties of heterocyclic [8]circulenes. Much of the interest in studying heterocyclic [8]circulenes stems from the planar cyclooctatetraene core often contained in these compounds, which in principle is antiaromatic. We start with a short introduction to the hydrocarbon [n]circulenes and proceed to describe the synthetic chemistry involved in creating tetraoxa[8]circulenes, with particular focus on the acid-mediated oligomerization of benzo- or naphthoquinones, resulting in some simple rules for predicting the outcome of the oligomerization reactions. These rules have guided the synthetic strategies for the preparation of azatrioxa[8]circulenes and diazadioxa[8]circulenes, which will be described in separate sections of this account. More traditional synthetic strategies have been applied in the preparation of octathia[8]circulene, tetrathiatetraselena[8]circulene, and a number of other heterocyclic [8]circulenes, and these synthetic efforts will be highlighted. Finally, a section describing structures that are closely related to the heterocyclic [8]circulenes will be presented, and at the end we will comment on the extensive theoretical work regarding the question of aromaticity/antiaromaticity of the central cyclooctatetraene of heterocyclic[8]circulenes. 1 Introduction 2 Synthesis of [n]circulenes 2.1 [4]Circulene 2.2 [5]Circulene 2.3 [6]Circulene 2.4 [7]Circulene 2.5 [8]Circulene 3 Synthesis of Tetraoxa[8]circulenes: A Historical Perspective 4 Synthesis of Azatrioxa[8]circulenes 5 Synthesis of Diazadioxa[8]circulenes 6 Synthesis of Other Heterocyclic [8]Circulenes 7 Synthesis of Structurally Related Compounds 8 Hetero[8]circulenes and Related Compounds as Tools to Study Aromaticity and Antiaromaticity 9 Conclusion and Outlook
引用
收藏
页码:498 / 525
页数:28
相关论文
共 96 条
[1]   Dithieno[3,4-b:3′,4′-d]thiophene-Annelated Antiaromatic Planar Cyclooctatetraene with Olefinic Protons [J].
Aita, Kazunari ;
Ohmae, Takeshi ;
Takase, Masayoshi ;
Nomura, Kotohiro ;
Kimura, Hideaki ;
Nishinage, Tohru .
ORGANIC LETTERS, 2013, 15 (14) :3522-3525
[2]   Silica-gel-supported ceric ammonium nitrate (CAN): A simple and efficient solid-supported reagent for oxidation of oxygenated aromatic compounds to quinones [J].
Ali, Mohammed Hashmat ;
Niedbalski, Melinda ;
Bohnert, Gary ;
Bryant, Daniel .
SYNTHETIC COMMUNICATIONS, 2006, 36 (12) :1751-1759
[3]  
Anthony J. W., 1990, HDB MINERALOGY, V5
[4]   DIPHENYLENES .2. SYNTHESES OF SUBSTITUTED DIPHENYLENES AND OF RELATED DIPHENYLS [J].
BAKER, W ;
BARTON, JW ;
MCOMIE, JFW .
JOURNAL OF THE CHEMICAL SOCIETY, 1958, (AUG) :2658-2665
[5]   The versatile thiophene: An overview of recent research on thiophene-based materials [J].
Barbarella, G ;
Melucci, M ;
Sotgiu, G .
ADVANCED MATERIALS, 2005, 17 (13) :1581-1593
[6]   DIBENZO[GHI,MNO]FLUORANTHENE [J].
BARTH, WE ;
LAWTON, RG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (02) :380-&
[7]   Electronic structure, aromaticity and spectra of hetero[8]circulenes [J].
Baryshnikov, G. V. ;
Minaev, B. F. ;
Minaeva, V. A. .
RUSSIAN CHEMICAL REVIEWS, 2015, 84 (05) :455-484
[8]   Aromaticity of the planar hetero[8]circulenes and their doubly charged ions: NICS and GIMIC characterization [J].
Baryshnikov, G. V. ;
Valiev, R. R. ;
Karaush, N. N. ;
Minaev, B. F. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (29) :15367-15374
[9]   Nucleus-independent chemical shift criterion for aromaticity in π-extended tetraoxa[8]circulenes [J].
Baryshnikov, Gleb V. ;
Minaev, Boris F. ;
Pittelkow, Michael ;
Nielsen, Christian B. ;
Salcedo, Roberto .
JOURNAL OF MOLECULAR MODELING, 2013, 19 (02) :847-850
[10]   Co-ordination polymers containing square grids of dimension 15 x 15 Å [J].
Biradha, K ;
Fujita, M .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 2000, (21) :3805-3810