...
首页> 外文期刊>Magnetic Resonance in Chemistry: MRC >~1H, ~(13)C, ~(15)N NMR coordination shifts in Fe(II), Ru(II) and Os(II) cationic complexes with 2,2~′:6~′,2~″- terpyridine
【24h】

~1H, ~(13)C, ~(15)N NMR coordination shifts in Fe(II), Ru(II) and Os(II) cationic complexes with 2,2~′:6~′,2~″- terpyridine

机译:Fe(II),Ru(II)和Os(II)与2,2〜':6〜',2〜''-三联吡啶的阳离子配合物中的〜1H,〜(13)C,〜(15)N NMR配位移位

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

~1H, ~(13)C and ~(15)N NMR studies of iron(II), ruthenium(II) and osmium(II) bis-chelated cationic complexes with 2,2~′:6~′,2~″-terpyridine ([M(terpy)_2]~(2+); M = Fe, Ru, Os) were performed. Significant shielding of nitrogen-adjacent H(6) and deshielding of H(3~′), H(4~′) protons were observed, both effects being mostly expressed for Fe(II) compounds. The metal-bonded nitrogens were shielded, this effect being much larger for the outer N(1), N(1~″) than the inner N(1~′) atoms, and enhanced in the Fe(II) → Ru(II) → Os(II) series.
机译:铁(II),钌(II)和(II)与2,2〜':6〜',2〜的双螯合阳离子配合物的〜1H,〜(13)C和〜(15)N NMR研究进行了-三联吡啶([M(terpy)_2]〜(2 +); M = Fe,Ru,Os)。观察到显着的氮相邻H(6)的屏蔽和H(3〜'),H(4'')质子的去屏蔽,这两种作用主要表现为Fe(II)化合物。金属键合的氮被屏蔽,外N(1),N(1〜'')的作用大于内N(1〜')原子,并在Fe(II)→Ru(II)中增强)→Os(II)系列。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号