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1.
近年来二茂铁及其衍生物的合成与应用研究是金属有机化学研究的热点.本文不仅对二茂铁及其衍生物的性质、合成及其应用研究现状作了归纳和评述,而且简要概括了二茂铁及其衍生物的未来研究方向.  相似文献   

2.
开环聚合制备高分子量聚二茂铁衍生物及其性能的研究   总被引:4,自引:0,他引:4  
王学杰  王立 《化学进展》2002,14(6):486-493
综述了近年来国内外高分子量聚二茂铁衍生物的研究进展。对热引发、阴离子引发、过渡金属催化等开环聚合方法及机理以及聚合物结构、性能及潜在应用作了介绍。  相似文献   

3.
二茂铁及其衍生物作为电化学传感器的研究进展   总被引:1,自引:0,他引:1  
本文对近二十年来国内外对二茂铁及其衍生物作为电化学传感器的研究进展做了较全面的综述。主要讨论了二茂铁及其衍生物修饰电极的制备、表征,介绍了二茂铁及其衍生物作为电化学传感器的应用情况,并探讨了今后的研究方向。  相似文献   

4.
采用化学聚合方法合成了一种含二茂铁电活性基团的新型导电聚噻吩衍生物聚3-[(二茂铁甲酸乙酯)三乙氧基]氧基噻吩, 用1H NMR和红外光谱等方法对其结构进行了表征. 实验结果表明, 该聚合物可溶于三氯甲烷、四氢呋喃和丙酮等有机溶剂, 并且二茂铁在聚合物中依然保持良好的氧化还原活性, 对钠离子具有良好的选择性络合作用.  相似文献   

5.
二茂铁酰基衍生物的研究进展   总被引:17,自引:2,他引:15  
时蕾  贾学顺 《合成化学》1998,6(2):137-149
综述了近年来二茂铁酰基衍生物如二茂铁甲醛、二茂铁酮和二茂铁甲酸的合成及反应的研究进展,简要介绍了它在生物学、医学和电化学等领域的应用。参考文献73篇。  相似文献   

6.
以二茂铁甲醛、1,1'-二茂铁二甲醛、2,6-二氨基吡啶、2-氨基-7-甲基-1,8-萘啶等为原料合成了二茂铁单臂和双臂衍生物Fe L1~Fe L4,并通过核磁共振氢谱、碳谱、质谱和元素分析等对衍生物的结构进行了表征和鉴定,同时用循环伏安法研究了四种衍生物的电化学性质.通过紫外可见分光光度法和核磁滴定,研究了四种衍生物与金属离子的相互作用.结果表明,二茂铁吡啶衍生物Fe L1和Fe L2能够在15种混合金属离子中特异性识别铜离子和铬离子,二茂铁萘啶衍生物Fe L3和Fe L4能够在15种混合金属离子中特异性识别铬离子,这种方法在体外环境污染监测和体内金属离子超标检测中都具有潜在的应用.  相似文献   

7.
李湘广  杨秉勤  谷利军  宁伟 《应用化学》2009,26(10):1184-1188
将二茂铁磺酰氯或二茂铁甲酰氯和1H-苯并咪唑衍生物反应,合成了12个未见文献报道的N-(酰基二茂铁)苯并咪唑类化合物,用IR、1HNMR、元素分析和MS对其结构进行了表征。结果表明,含有活泼氢的苯并咪唑衍生物能与二茂铁酰氯生成相应的N-(酰基二茂铁)苯并咪唑衍生物,并有较好的收率。  相似文献   

8.
半个世纪以来,由于二茂铁及其衍生物表现出特有的芳香性、稳定性、氧化还原性及生物活性等,使得它们在材料、航天、医疗等领域得到了广泛的应用。醛基取代二茂铁衍生物是其中的重要一种,除了具有二茂铁的特性外,还具有醛基的还原性以及羰基和Cp环的共轭特征,使其成为重要的中间体或起始原料,例如:Wright课题组首次合成了主链含二茂铁的二阶非线形金属有机聚合物,  相似文献   

9.
由季铵盐合成有机胂二茂铁衍生物杜洪光,师树简(北京化工大学应用化学系,北京,100029)关键词有机胂,二茂铁衍生物,铵甲碘化物,亲核取代关于二茂铁季铵盐的亲核取代反应已有较多报道[1~4],但对于含胂二茂铁季铵盐的这类反应还未见诸文献,由碘化[2-...  相似文献   

10.
平面手性二茂铁衍生物已经发展成为不对称催化反应中一类良好的手性配体和手性催化剂.高效、高对映选择性的平面手性二茂铁衍生物合成方法研究是不对称催化研究的热点之一.综述了近年来利用过渡金属催化法合成面手性二茂铁衍生物的进展.  相似文献   

11.
In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.  相似文献   

12.
KMnO4-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.  相似文献   

13.
The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.  相似文献   

14.
Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.  相似文献   

15.
The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.  相似文献   

16.
A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.  相似文献   

17.
The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp3)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp2)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp2)?H and aliphatic 1,5- and 1,6-C(sp3)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp3)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp2)?H insertion.  相似文献   

18.
An efficient approach to the synthesis of highly congested di, penta and hexacyclic pyrazoles as well as imidazole fragment containing novel heterocyclic molecule has been developed through a carbanion induced transformation of suitably functionalized 2H-pyran-2-ones, benzo[h]chromene and thiochromeno[4,3-b]pyrans. Due to the presence of fluorescence, we report their prime application metal sensor as off/on switching in ferric ions.  相似文献   

19.
Zhanhui Yang  Shiyi Yang  Jiaxi Xu 《Tetrahedron》2017,73(23):3240-3248
Regiospecific and direct imidation of the methyl C(sp3)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products.  相似文献   

20.
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