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首页> 外文期刊>Journal of Fluorine Chemistry >Synthesis and characterization of novel 2-fluoro/chloro-3-pyridyl selenides: X-ray crystal structure of bis(2-fluoro-3-pyridyl) diselenide and bis(2-fluoro-3-pyridylseleno) methane
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Synthesis and characterization of novel 2-fluoro/chloro-3-pyridyl selenides: X-ray crystal structure of bis(2-fluoro-3-pyridyl) diselenide and bis(2-fluoro-3-pyridylseleno) methane

机译:新型2-氟/氯-3-吡啶基硒化物的合成与表征:双(2-氟-3-吡啶基)二硒化物和双(2-氟-3-吡啶基硒代)甲烷的X射线晶体结构

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摘要

An efficient one-pot synthesis of bis(2-fluoro/chloro-3-pyridyl) diselenide has been successfully achieved under dry-ice/acetone bath temperature that involves deprotonation of corresponding 2-fluoro/chloropyridine at C-3 with lithium di-isopropylamide, insertion of elemental selenium followed by the subsequent aerial oxidation. A series of novel and synthetically important unsymmetrical 2-fluoro/2-chloro substituted alkyl/allyl/benzyl pyridyl selenium compounds and a diselenoacetal, bis(2-fluoro-3-pyridylseleno) methane have been prepared by the reductive cleavage of the titled bis(2-fluoro/ chloro-3-pyridyl) diselenides with sodium borohydride followed by quenching with the appropriate alkylating agents. The same could be realized by the deprotonation of 2-halopyridine accompanied with the insertion of elemental selenium followed by addition of appropriate alkylating agents. The hitherto unknown compounds have been fully characterized by elemental analysis and various spectroscopic techniques i.e., FT-IR, multinuclear (~1H, ~(13)C, ~(19)F and ~(77)Se) NMR and mass spectrometry. The crystal structures of bis(2-fluoro-3-pyridyl) diselenide and bis(2-fluoro-3-pyridylseleno) methane have been determined by single crystal X-ray diffraction (XRD).
机译:在干冰/丙酮浴温度下成功地完成了一锅法合成双(2-氟/氯-3-吡啶基)二硒化物的有效反应,该过程涉及在相应的温度下在C-3下用二锂锂对相应的2-氟/氯吡啶进行去质子处理。异丙酰胺,插入元素硒,然后进行随后的空中氧化。通过标题化合物“ bis”的还原裂解,制备了一系列新颖且在合成上很重要的不对称的2-氟/ 2-氯取代的烷基/烯丙基/苄基吡啶基硒化合物和二硒缩醛双(2-氟-3-吡啶基硒代)甲烷。 (2-氟/氯-3-吡啶基)二硒化物与硼氢化钠,然后用适当的烷基化剂淬灭。通过将2-卤代吡啶去质子化并插入元素硒,然后加入适当的烷基化剂,可以实现相同的目的。迄今未知的化合物已通过元素分析和各种光谱技术(即FT-IR,多核(〜1H,〜(13)C,〜(19)F和〜(77)Se)NMR和质谱)进行了全面表征。双(2-氟-3-吡啶基)二硒化物和双(2-氟-3-吡啶基硒代)甲烷的晶体结构已经通过单晶X射线衍射(XRD)确定。

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