Cyclodiphosphazanes with functionalities: Synthesis, reactivity and transition metal chemistry

被引:26
作者
Balakrishna, Maravanji S. [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Phosphorus Lab, Bombay 400076, Maharashtra, India
关键词
Cyclodiphosphazanes; Donor functionalities; Transition metal complexes; Macrocycles; Coordination polymers; Bidentate ligands; STRUCTURAL-CHARACTERIZATION; MOLECULAR-STRUCTURES; HETEROMETALLIC COMPLEXES; COORDINATION CHEMISTRY; COPPER(I) COORDINATION; REVERSIBLE CONVERSION; METHYLENE INSERTION; MACROCYCLE; CRYSTAL; CIS-((O-MEOC6H4O)P(MU-(NBU)-BU-T))(2);
D O I
10.1016/j.jorganchem.2009.11.024
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The saturated, four-membered rings of the type [XP(mu-NR)] 2 containing alternating phosphorus(III) and nitrogen atoms are known as cyclodiphosphazanes or diazadiphosphetidines. The current interest in these well-known heterocycles is due to their catalytic and biological applications besides their excellent synthetic utility as scaffolds to design interesting macrocycles with or without involving main group or transition metals. Although the rigid and nearly-planar neutral P(2)N(2) rings resemble [Cu(mu-X)](2) (X = Cl, Br or I) rhombic units ([Cu(mu-X)](2) are known for giving a variety of structures with suitable ligands), their utility in designing the high-nuclearity clusters, cages or coordination polymers is scarce. In this context, we fine tuned the coordinating ability of these ligands by incorporating pendant hemi-labile functionalities on phosphorus centers which resulted in the isolation of several interesting molecules. The details are described. (C) 2009 Elsevier B. V. All rights reserved.
引用
收藏
页码:925 / 936
页数:12
相关论文
共 47 条
[1]   Bis(imino)cyclodiphosph(V)azane complexes of late transition metals:: Efficient catalyst precursors for ethene and propene oligomerization and dimerization [J].
Axenov, KV ;
Leskelä, M ;
Repo, T .
JOURNAL OF CATALYSIS, 2006, 238 (01) :196-205
[2]   Bis(amido)cyclodiphosph(III)azane hafnium complexes and their activation by tris(perfluorophenyl)borane [J].
Axenov, KV ;
Klinga, M ;
Leskelä, M ;
Repo, T .
ORGANOMETALLICS, 2005, 24 (06) :1336-1343
[3]   Functionalized cyclodiphosphazanes cis-[tBuNP(OR)]2 (R=C6H4OMe-o, CH2CH2OMe, CH2CH2SMe, CH2CH2NMe2) as neutral 2e, 4e or 8e donor ligands [J].
Balakrishna, Maravanji S. ;
Chandrasekaran, P. ;
Venkateswaran, Ramalingam .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2007, 692 (13) :2642-2648
[4]   Synthesis and molecular structure of 1,3-di-tert-butyl-2,4-bis(cyclodipentadienyl)iron(II) 1,3,2,4-diazadiphosphetidine, [Fe(η5-C5H4)2(PNtBu)2] [J].
Balakrishna, Maravanji S. ;
Mague, Joel T. .
ORGANOMETALLICS, 2007, 26 (18) :4677-4679
[5]   Chemistry of pnictogen(III)-nitrogen ring systems [J].
Balakrishna, Maravanji S. ;
Eisler, Dana J. ;
Chivers, Tristram .
CHEMICAL SOCIETY REVIEWS, 2007, 36 (04) :650-664
[6]   Cyclodiphosphazanes with functionalities: Synthesis, reactivity and transition metal chemistry [J].
Balakrishna, Maravanji S. .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2010, 695 (07) :925-936
[7]   An Acyclic Dimer of Cyclodiphosphazane {tBuHN(tBuNP)2OCH2}2 Containing Alkoxo and Amido Functionalities: Synthesis, Derivatization, Bi- (PdII, RhI), and Tetranuclear (PdII, AuI, RhIAuI) Transition Metal Complexes [J].
Balakrishna, Maravanji S. ;
Venkateswaran, Rarnalingam ;
Mague, Joel T. .
INORGANIC CHEMISTRY, 2009, 48 (04) :1398-1406
[8]   COORDINATION CHEMISTRY OF DIPHOSPHINOAMINE AND CYCLODIPHOSPHAZANE LIGANDS [J].
BALAKRISHNA, MS ;
REDDY, VS ;
KRISHNAMURTHY, SS ;
NIXON, JF ;
STLAURENT, JCTRB .
COORDINATION CHEMISTRY REVIEWS, 1994, 129 (1-2) :1-90
[9]   Theoretical investigations on chalcogen-chalcogen interactions:: What makes these nonbonded interactions bonding? [J].
Bleiholder, C ;
Werz, DB ;
Köppel, H ;
Gleiter, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (08) :2666-2674
[10]  
Blue ED, 2002, ANGEW CHEM INT EDIT, V41, P2571, DOI 10.1002/1521-3773(20020715)41:14<2571::AID-ANIE2571>3.0.CO