Hartwick Christopher J, Yelgaonkar Shweta P, Reinheimer Eric W, Campillo-Alvarado Gonzalo, MacGillivray Leonard R
Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, United States.
Rigaku Oxford Diffraction, 9009 New Trails Drive, The Woodlands, Texas 77381, United States.
Cryst Growth Des. 2021 Aug 4;21(8):4482-4487. doi: 10.1021/acs.cgd.1c00382. Epub 2021 Jul 13.
Self-assembled complexes utilizing the ditopic dative bond acceptor 1,3-diboronic acid with catechol and complementary U-shaped donors in the form of 1,8-dipyridylnaphthalenes (1,8-bis(4-pyridyl)naphthalene (), 1,8-bis(4-ethylenylpyridyl)naphthalene (), and 1,8-bis(4-ethynylpyridyl)naphthalene ()) yielded discrete two-component structures. The assemblies exhibit "plug-in-socket" geometries. DFT calculations are consistent with the donor pyridyl and acceptor catecholate being electron poor and rich, respectively. The assemblies pack via π-π interactions and support the inclusion of a solvent (i.e., , ). The materials may form a basis for the design of complex B-based structures (e.g., supramolecular dyads).
利用双齿配位键受体1,3 - 二硼酸与儿茶酚以及呈1,8 - 二吡啶基萘(1,8 - 双(4 - 吡啶基)萘( )、1,8 - 双(4 - 乙烯基吡啶基)萘( )和1,8 - 双(4 - 乙炔基吡啶基)萘( )形式的互补U形供体自组装形成离散的二元结构。这些组装体呈现出“插头 - 插座”几何形状。密度泛函理论计算结果与供体吡啶基和受体儿茶酚盐分别为缺电子和富电子的情况一致。这些组装体通过π - π相互作用堆积,并支持溶剂(即 , )的包合。这些材料可能为基于配合物B的结构(例如超分子二元体)的设计奠定基础。