搜索结果: 16-28 共查到“有机化学 NMR”相关记录28条 . 查询时间(0.015 秒)
摘要 应用~1H, ~(13)C和~(51)V多核NMR技术和电喷雾质谱等谱学手段研究草酸双过 氧钒配合物与吡啶、4-甲基咪唑、咪唑等有机配体的相互作用。研究发现:这些 相互作用都生成过氧钒物种[OV(O_2)_2L]~-(L为有机配体),其从易到难的顺序 为咪唑>4-甲基咪唑>吡啶。当配体为4-甲基咪唑时,产物是一对未见报道的异 构体。研究结果表明:将NMR技术和电喷雾质谱有机结合是研究此类体系...
2-甲硫基-7(5)-取代-3-吡唑并[1,5-a]嘧啶甲酸乙酯的区域选择性合成与2D NMR 研究
吡唑并[1,5-a吡唑并[1,5-a]嘧啶 二维核磁 反应机理 区域选择性 合成
2007/12/19
摘要 利用3-甲硫基-4-乙氧羰基-5-氨基-1H-吡唑分别与甲基/芳基烯胺酮反应, 合成了8种新的化合物2-甲硫基-7-取代-3-吡唑并[1,5-a]嘧啶甲酸乙酯(3a~3g)和2-甲硫基-5-甲基-3-吡唑并[1,5-a]嘧啶甲酸乙酯(4a). 化合物的结构均经元素分析, IR, 1H NMR, MS所证实, 异构体3a和4a的结构进一步由13C NMR, HMQC和HMBC确认. 同时, 探...
摘要 2-{2-[4-苯基-二(4-特丁基苯基)甲基]苯氧基}乙氧乙醇磺酸酯(1)与4,4'-联吡啶在乙腈中回流36 h, 随后通过阴离子交换得到N-{2-{2-[4-苯基-二(4-特丁基苯基)甲基]苯氧基}乙氧乙基}-4,4'-联吡啶六氟磷酸盐(3), 产率为93.4%. 3与4,4'-二(溴甲基)-2,2'-联吡啶在乙腈中、70 ℃下反应72 h, 生成哑铃型化合物5, 产率为45%. 5与冠...
通过对二十三个香茶菜植物中二萜类化合物的1HNMR 参数的归纳, 总结了这些化合物的主要质子信号的规律, 用分子模型使分子立体结构(B,C 环构象和取代基构型)与峰形相关连, 为此类化合物的签别和结构确定提供了依据.
NMR位移试剂Eu(fod)~4^-对锍盐^1H和^1^3C NMR的影响
核磁共振谱法 碳13核磁共振谱法 铕化合物 氟硼酸 有机合成 位移试剂 锍化合物 结构表征 煤炭系统留学回国人员科技基金
2007/12/13
合成了八种新的四氟硼酸二甲基苯基锍,用元素分析和核磁共振对其结构进行了表征。研究了以CDCl~3为溶剂,NMR位移试剂Eu(fod)~4^-对所合成锍盐的^1H和^1^3C NMR的影响。结果表明,Eu(fod)~4^-是一个对锍盐非常有效的位移试剂,且Eu(fod)~4^-对二甲基苯基锍盐之甲基的^1H和^1^3C NMR的位移呈线性关系。
有机磷化合物的NMR研究I.苯并[1,3,2]氧氮磷杂环己-4-酮衍生物的^1H,^3^1P和^1^3CNMR谱
核磁共振谱 碳13核磁共振谱法 氮杂环化合物 有机磷化合物 质子磁共振谱法 氧杂环化合物 化学位移 磷杂环化合物
2007/12/10
The 1H, 31P, and 13C NMR parameters of 1,3,2-benzoxazaphosphorin-4-one derivatives I [R = heterocyclyl; R1 = OEt, NMe2, (ClCH2CH2)2N, (ICH2CH2)2N; X = O, S] have been studied. Effects of chiral phosph...
本文报道了十个不对称取代1,3,2-二氮磷杂环戊烷的^1^3C核磁共振谱, 利用^1^3C自旋-晶格弛豫时间确定了用其它去偶技术难以确定的信号的归属, 讨论了偶合常数与构象的关系.
Development of a New Set of Additive Parameters for the Estimation of Geometrical Distortion of Cycloalkanes from C-13 NMR Chemical Shifts
Additivity parameters C-13 NMR chemical shifts geometrical distortion cycloalkanes
2010/4/16
A previous model for the calculation of C-13 chemical shifts is modified by replacement of 3 parameters representing the p-character of carbon atom in cyclic systems with a single parameter aiming for...
Investigation of the Cation Complexation by Macrocyclic Ethers using 13C NMR Spin--Lattice Dipolar Relaxation Time Measurements
Investigation the Cation Complexation Macrocyclic Ethers using 13C NMR Spin--Lattice Dipolar Relaxation
2010/4/19
The binding constants (Ka) of [18]crown-6 ether with Na+ , K+, and Ba2+ thiocyanates were determined by 13C{1H} NMR spin--lattice dipolar relaxation time measurements. The observed relaxation times (T...
Synthesis of 2-[2-(3,4,5-Trimethoxybenzoyloxy)ethyl]pyrrolidine Hydrochloride Controlled by GC-MS, 1H and 13C NMR Analyses
2-[2-(3,4,5-trimethoxybenzoyloxy)ethyl]pyrrolidine hydrochloride pyrrolidine derivatives O-acylation of amino alcohols removal of Cbz group
2010/4/19
The synthesis of 2-[2-(3,4,5-trimethoxybenzoyloxy)ethyl]pyrrolidine hydrochloride was performed using 2-(2-hydroxyethyl)pyrrolidine as a starting material. Before the O-acylation reaction with 3,4,5-t...
1H, 13C, 119Sn NMR, Mass, Mössbauer and Biological Studies of Tri-,Di- and Chlorodiorganotin(IV) Carboxylates
1H 13C 119Sn NMR Mass Mö ssbauer Biological Studies
2010/4/21
The reaction of 2-[(2,3-dimethylphenyl)amino]benzoic acid (HL) with tri- and diorganotin(IV) chlorides yielded complexes of the type R3SnL and R2SnL2 (R = n-C4H9, C6H5, C6H5CH2, n-C8H17). The compound...
13C-and 31P-NMR Study of Tetracarbonylbis(diphenylphosphino)alkanemetal(0) Complexes of The Group 6 Elements
Chromium Molybdenum Tungsten Carbonyl Diphosphine NMR
2010/6/29
Tetracarbonylbis(diphenylphosphino)alkanemetal(0) complexes of the general formula M(CO)4[(C6H5)2P (CH2)nP(C6H5)2] (M: Cr, Mo, W; n: 1, 2, 3) were synthesized from the reaction of M(CO)4(h2:2-1,5-cycl...