Azide Groups in Higher Oxidation State Manganese Cluster Chemistry: From Structural Aesthetics to Single-Molecule Magnets
作者:Theocharis C. Stamatatos、George Christou
DOI:10.1021/ic801217j
日期:2009.4.20
long-established areas, manganese/oxo coordination cluster chemistry involving the higher MnII/MnIV oxidation states and transition-metal azide (N3−) chemistry. The combination of azide and alkoxide- or carboxylate-containing ligands in Mn chemistry has led to a variety of new polynuclear clusters, high-spin molecules, and single-molecule magnets, with metal nuclearities ranging from Mn4 to Mn32 and with
这个论坛文章概述了最近的两个长既定地区,锰/氧代涉及更高的Mn协调集群化学融合II / Mn为IV氧化态和过渡金属叠氮化物(N 3 - )的化学反应。锰化学中叠氮化物和含醇盐或羧酸盐的配体的组合导致了许多新的多核簇,高自旋分子和单分子磁体,其金属核范围从Mn 4到Mn 32,并且具有状态自旋值一样大的小号= 83 / 2。将有机桥接/螯合配位体是分别论述为如下:(i)吡啶基醇盐[2-(羟甲基)吡啶(哼),2,6- pyridinedimethanol的阴离子(pdmH 2),和宝石的二醇二-形式2-吡啶基酮(dpkdH 2)];(ii)非吡啶基醇盐[1,1,1-三(羟甲基)乙烷(thmeH 3),三乙醇胺(teaH 3)和N-甲基二乙醇胺(mdaH 2)的阴离子];(iii)其他醇类[2,6-二羟甲基-4-甲基苯酚(LH 3)和席夫碱];(iv)吡啶基一肟/二肟[甲基-2-吡啶基酮肟(mp