首页> 外文学位 >Tridentate nitrogen ligands derived from 2,6-bis-hydrazinopyridine (BHP): Preparation and study of the 2,6-bis-hydrazonopyridines, 2,6-bis-pyrazolylpyridines, and 2,6-bis-indazolylpyridines.
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Tridentate nitrogen ligands derived from 2,6-bis-hydrazinopyridine (BHP): Preparation and study of the 2,6-bis-hydrazonopyridines, 2,6-bis-pyrazolylpyridines, and 2,6-bis-indazolylpyridines.

机译:源自2,6-双-肼基吡啶(BHP)的三齿氮配体:2,6-双-肼基吡啶,2,6-双-吡唑基吡啶和2,6-双-吲唑基吡啶的制备和研究。

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摘要

The development of ligands for asymmetric catalysis has been a focal point in our research group. Tridentate nitrogen ligands have been used in a variety of asymmetric catalytic reactions. Of these, the 2,6-bis-pyrazolylpyridine class of ligands has found only limited use, due to difficulties in the normal synthetic route that limit the synthesis of ligands with bulky chiral groups attached to the pyrazole rings. The chiral derivatives that have been used in catalysis have shown modest to poor results, due in part to limitations in the synthesis of these ligands that prevent the development of bulky, chiral ligands.;A new synthetic route has been developed using 2,6-bis-hydrazinopyridine (BHP). This route allows for a facile, one-pot synthesis of 2,6-bis-pyrazolylpyridines that is not limited by the bulkiness of the groups that become attached to the pyrazole ring. The primary focus of this research has been the development of new chiral 2,6-bis-pyrazolylpyridines and an investigation into the limitations of steric bulk on chelation ability in this class of ligands. For this purpose, several novel chiral ligands have been synthesized. The effect of sterics and electronics on the regioselectivity of the formation of the pyrazole ring was also studied in order to develop more regioselective routes to this class of ligands. The new bulky pyrazolylpyridine ligands that have been synthesized using this route have also been tested for the ability to sucessfully coordinate a transition metal. This study lead to a better understanding of the limitations the size of the substitutents attached to pyrazole ring have on the ligands' ability to chelate metals.;While BHP was developed primarily for the synthesis of the 2,6-bis-pyrazolylpyridine class of ligands, its use has now been expanded to the synthesis of other classes of tridentate-nitrogen ligands, many of which would be diffiuclt or impossible to synthesize through any other route. Using this new methodolgy, the syntheses of two novel classes of ligands, each with unique properties, the 2,6-bis-hydrazonopyridines and 2,6-bis-indazolylpyridines, have now been accomplished. The previously unknown 2,6-bis-indazolylpyridine class of ligands is offers the possibility to synthesize more robust catalysts than is possible using the bis-pyrazole ligands because of the electronic nature of the indazole ring.
机译:用于不对称催化的配体的开发一直是我们研究小组的重点。三齿氮配体已用于各种不对称催化反应中。其中,由于在常规合成途径中的困难,其限制了具有连接到吡唑环的庞大手性基团的配体的合成,因此仅发现了有限的2,6-双吡唑基吡啶类配体。已用于催化的手性衍生物已显示出中等至较差的结果,部分原因是这些配体的合成受到限制,阻止了庞大的手性配​​体的发展。双肼基吡啶(BHP)。该途径允许2,6-双-吡唑基吡啶的容易的一锅合成,而不受与吡唑环连接的基团的庞大性的限制。这项研究的主要重点是开发新的手性2,6-双-吡唑基吡啶,并研究了在这种配体中空间体积对螯合能力的限制。为此目的,已经合成了几种新颖的手性配体。还研究了空间和电子学对吡唑环形成的区域选择性的影响,以开发针对这类配体的更多区域选择性途径。还已经测试了使用该途径合成的新的庞大的吡唑基吡啶配体的成功配位过渡金属的能力。这项研究使人们更好地理解了与吡唑环相连的取代基的大小对配体螯合金属的能力的限制。;虽然BHP主要用于合成2,6-双吡唑基吡啶类配体目前,其用途已扩展到合成其他种类的三齿氮配体,其中许多配体将很难或无法通过任何其他途径合成。使用这种新方法,现已完成了两类具有独特性质的新型配体的合成,分别是2,6-双-肼基吡啶和2,6-双-吲哚基吡啶。由于吲唑环的电子性质,与使用双-吡唑配体相比,以前未知的2,6-双-吲唑基吡啶类配体提供了合成更坚固催化剂的可能性。

著录项

  • 作者

    Duncan, Nathan C.;

  • 作者单位

    Baylor University.;

  • 授予单位 Baylor University.;
  • 学科 Chemistry Organic.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 255 p.
  • 总页数 255
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

  • 入库时间 2022-08-17 11:38:05

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