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本文引用的文献

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Template-Directed Self-Recognition of Alkyl-Bridged Bis(catechol) Ligands in the Formation of Helicate-Type Complexes.在螺旋型配合物形成过程中烷基桥连双(儿茶酚)配体的模板导向自识别
Angew Chem Int Ed Engl. 1999 Feb 15;38(4):557-559. doi: 10.1002/(SICI)1521-3773(19990215)38:4<557::AID-ANIE557>3.0.CO;2-S.
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Ligand Self-Recognition in the Self-Assembly of a [{Cu(L)} ] Complex: The Role of Chirality.[{Cu(L)}]配合物自组装过程中的配体自识别:手性的作用。
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Synthesis of a new family of hexakisferrocenyl hexagons and their electrochemical behavior.新型六联二茂铁基六边形分子的合成及其电化学行为
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Self-selection in the self-assembly of isomeric supramolecular squares from unsymmetrical bis(4-pyridyl)acetylene ligands.由不对称双(4-吡啶基)乙炔配体自组装异构超分子正方形中的自选择。
J Org Chem. 2008 Sep 5;73(17):6580-6. doi: 10.1021/jo800957r. Epub 2008 Aug 7.
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Size selective self-sorting in coordination-driven self-assembly of finite ensembles.有限聚集体配位驱动自组装中的尺寸选择性自分类
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Coordination-driven self-assembly of cavity-cored multiple crown ether derivatives and poly[2]pseudorotaxanes.基于配位作用的腔核多冠醚衍生物与聚[2]准轮烷的自组装
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Functionalized hydrophobic and hydrophilic self-assembled supramolecular rectangles.功能化的疏水和亲水自组装超分子矩形。
J Org Chem. 2008 Mar 7;73(5):1787-94. doi: 10.1021/jo702380b. Epub 2008 Feb 2.
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A new family of multiferrocene complexes with enhanced control of structure and stoichiometry via coordination-driven self-assembly and their electrochemistry.通过配位驱动自组装对结构和化学计量比具有增强控制作用的新型多铁茂配合物家族及其电化学性质
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9
A highly efficient approach to the self-assembly of hexagonal cavity-cored tris[2]pseudorotaxanes from several components via multiple noncovalent interactions.一种通过多种非共价相互作用,由多种组分自组装形成具有六边形空穴核心的三[2]准轮烷的高效方法。
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配位驱动自组装中的二阶自组织:探索自我选择的极限

Second-order self-organization in coordination-driven self-assembly: exploring the limits of self-selection.

作者信息

Northrop Brian H, Yang Hai-Bo, Stang Peter J

机构信息

University of Utah, Department of Chemistry, 315 South 1400 E, Salt Lake City, Utah 84112, USA.

出版信息

Inorg Chem. 2008 Dec 1;47(23):11257-68. doi: 10.1021/ic801711q.

DOI:10.1021/ic801711q
PMID:18980302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2650397/
Abstract

Self-organization during the self-assembly of a series of functionalized bispyridyl organic donors with complementary di-Pt(II) acceptors into supramolecular rhomboids and rectangles is explored. The connectivity and location of functional groups on the organic donors ensures that they do not interfere sterically or electronically with their respective binding sites. Carefully controlled reaction conditions are employed so that the only means of self-organization during self-assembly is through "second-order" effects arising from the distal functional groups themselves. With the selection of functionalized systems studied, the extent of second-order self-organization varies from essentially zero to quite pronounced.

摘要

探索了一系列带有互补二价铂(II)受体的功能化联吡啶有机供体自组装成超分子菱形和矩形过程中的自组织现象。有机供体上官能团的连接性和位置确保它们在空间或电子方面不会干扰各自的结合位点。采用精心控制的反应条件,使得自组装过程中自组织的唯一方式是通过远端官能团自身产生的“二阶”效应。在所研究的功能化体系中,二阶自组织的程度从基本为零到相当显著不等。