Tuning selenium-iodine contacts:: from secondary soft-soft interactions to covalent bonds

被引:65
作者
du Mont, WW
Martens-von Salzen, A
Ruthe, F
Seppälä, E
Mugesh, G
Devillanova, FA
Lippolis, V
Kuhn, N
机构
[1] Tech Univ, Inst Anorgan & Analyt Chem, D-38106 Braunschweig, Germany
[2] Complesso Univ Monserrato, Dipartimento Chim Inorgan & Analit, I-09042 Monserrato, CA, Italy
[3] Univ Tubingen, Inst Anorgan Chem, D-72076 Tubingen, Germany
关键词
selenium; iodine; hypervalency; supramolecular structures; soft-soft interactions;
D O I
10.1016/S0022-328X(00)00665-3
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Selenium to iodine contacts ranging from the sum of the Se and I van der Waals distances to strong covalent bonds are reviewed with the help of recent structural determinations of compounds exhibiting Se-I distances from 384 to 244 pm, with emphasis on 'less clear-cut' cases, in terms of different extents of 'hypervalent' 3c-4e (10-Se-3) and (10-I-2) interactions. Within a continuum of Se-I interactions from undisturbed single bonds via n- > sigma*(Se-I) interactions and typical 3c-4e X-Se-I or Se-I-X systems to van der Waals contacts, any desired Se-I distances can be tuned by an appropriate choice of the particular substituents and ligands attached to the Se-I moiety. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:14 / 28
页数:15
相关论文
共 96 条
[1]   Electrochemical synthesis of tetrakis [N-methylbenzothiazole-2(3H)-selone]selenium(2+)tetrafluoroborate: An uncommon dication containing the mixed-valence Se-5 framework [J].
Adamo, C ;
Demartin, F ;
Deplano, P ;
Devillanova, FA ;
Isaia, F ;
Lelj, F ;
Lippolis, V ;
Lukes, P ;
Mercuri, ML .
CHEMICAL COMMUNICATIONS, 1996, (07) :873-874
[2]   Charge-transfer adducts between donors containing chalcogens (S and Se) and di-iodine: solution studies [J].
Aragoni, MC ;
Arca, M ;
Devillanova, FA ;
Garau, A ;
Isaia, F ;
Lippolis, V ;
Verani, G .
COORDINATION CHEMISTRY REVIEWS, 1999, 184 :271-290
[3]   Reactivity of 1,3,5-trithiacyclohexane and 1,3,5-triselenacyclohexane towards molecular diiodine. Crystal structures of the diiodine adducts [J].
Arca, M ;
Cristiani, F ;
Devillanova, FA ;
Garau, A ;
Isaia, F ;
Lippolis, V ;
Verani, G ;
Demartin, F .
POLYHEDRON, 1997, 16 (12) :1983-1991
[4]   [RE2I2(CO)(6)(SE-7)], A COORDINATION COMPOUND OF ELEMENTAL SELENIUM WITH A TRANSITION-METAL - A SOLUTION AND SOLID-STATE STUDY [J].
BACCHI, A ;
BARATTA, W ;
CALDERAZZO, F ;
MARCHETTI, F ;
PELIZZI, G .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1994, 33 (02) :193-195
[5]   STRUCTURAL CHEMISTRY OF DONOR-ACCEPTOR INTERACTIONS [J].
BENT, HA .
CHEMICAL REVIEWS, 1968, 68 (05) :587-&
[6]  
BERRY MJ, 1991, J BIOL CHEM, V266, P14155
[7]   TYPE-I IODOTHYRONINE DEIODINASE IS A SELENOCYSTEINE-CONTAINING ENZYME [J].
BERRY, MJ ;
BANU, L ;
LARSEN, PR .
NATURE, 1991, 349 (6308) :438-440
[8]  
BIGOLI F, 1994, GAZZ CHIM ITAL, V124, P445
[9]   REACTION OF BIS(MORPHOLINOSELENOCARBONYL) TRISELENIDE WITH IODINE - EXISTENCE OF A 1-1 CHARGE-TRANSFER PRECURSORY ADDUCT IN SOLUTION IN AN OXIDATIVE REACTION - ISOLATION AND CRYSTAL-STRUCTURE OF THE NEW (N-MORPHOLINECARBODISELENOATO)SELENIUM(II) IODIDE [J].
BIGOLI, F ;
LEPORATI, E ;
PELLINGHELLI, MA ;
CRISPONI, G ;
DEPLANO, P ;
TROGU, EF .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1983, (08) :1763-1769
[10]   Synthesis, characterization, and crystal structures of new dications bearing the -Se-Se- bridge [J].
Bigoli, F ;
Demartin, F ;
Deplano, P ;
Devillanova, FA ;
Isaia, F ;
Lippolis, V ;
Mercuri, ML ;
Pellinghelli, MA ;
Trogu, EF .
INORGANIC CHEMISTRY, 1996, 35 (11) :3194-3201