Design and construction of supramolecular polysulfurated metallodendrimers with various shapes and sizes via coordination-driven self-assembly

Nai Wei Wu; Quan Jie Li; Jing Zhang; Jiuming He; Jiang Kun Ou-Yang; Hongwei Tan; Zeper Abliz; Hai Bo Yang

doi:10.1016/j.tet.2013.04.058

Design and construction of supramolecular polysulfurated metallodendrimers with various shapes and sizes via coordination-driven self-assembly

Nai Wei Wu
, Quan Jie Li
, Jing Zhang
, Jiuming He
, Jiang Kun Ou-Yang
, Hongwei Tan
, Zeper Abliz
, Hai Bo Yang^*

^*此作品的通讯作者

化学与分子工程学院

East China Normal University
Beijing Normal University
Chinese Academy of Medical Sciences

科研成果: 期刊稿件 › 文章 › 同行评审

17 引用（Scopus）

摘要

A new family of 120 polysulfurated dipyridine donors have been successfully designed and synthesized, from which a series of novel rhomboidal and hexagonal supramolecular polysulfurated metallodendrimers were prepared via coordination-driven self-assembly. The structures of the newly designed polysulfurated metallodendrimers were characterized by multinuclear NMR ( ¹H and ³¹P), mass spectrometry (CSI-TOF-MS), and elemental analysis. Moreover, the shape and size of these novel metallodendrimers were investigated with PM6 semi-empirical molecular orbital methods.

源语言	英语
页（从-至）	5981-5988
页数	8
期刊	Tetrahedron
卷	69
期	29
DOI	https://doi.org/10.1016/j.tet.2013.04.058
出版状态	已出版 - 22 7月 2013

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abstract = "A new family of 120 polysulfurated dipyridine donors have been successfully designed and synthesized, from which a series of novel rhomboidal and hexagonal supramolecular polysulfurated metallodendrimers were prepared via coordination-driven self-assembly. The structures of the newly designed polysulfurated metallodendrimers were characterized by multinuclear NMR ( 1H and 31P), mass spectrometry (CSI-TOF-MS), and elemental analysis. Moreover, the shape and size of these novel metallodendrimers were investigated with PM6 semi-empirical molecular orbital methods.",

author = "Wu, \{Nai Wei\} and Li, \{Quan Jie\} and Jing Zhang and Jiuming He and Ou-Yang, \{Jiang Kun\} and Hongwei Tan and Zeper Abliz and Yang, \{Hai Bo\}",

year = "2013",

month = jul,

day = "22",

doi = "10.1016/j.tet.2013.04.058",

language = "英语",

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T1 - Design and construction of supramolecular polysulfurated metallodendrimers with various shapes and sizes via coordination-driven self-assembly

AU - Wu, Nai Wei

AU - Li, Quan Jie

AU - Zhang, Jing

AU - He, Jiuming

AU - Ou-Yang, Jiang Kun

AU - Tan, Hongwei

AU - Abliz, Zeper

AU - Yang, Hai Bo

PY - 2013/7/22

Y1 - 2013/7/22

N2 - A new family of 120 polysulfurated dipyridine donors have been successfully designed and synthesized, from which a series of novel rhomboidal and hexagonal supramolecular polysulfurated metallodendrimers were prepared via coordination-driven self-assembly. The structures of the newly designed polysulfurated metallodendrimers were characterized by multinuclear NMR ( 1H and 31P), mass spectrometry (CSI-TOF-MS), and elemental analysis. Moreover, the shape and size of these novel metallodendrimers were investigated with PM6 semi-empirical molecular orbital methods.

AB - A new family of 120 polysulfurated dipyridine donors have been successfully designed and synthesized, from which a series of novel rhomboidal and hexagonal supramolecular polysulfurated metallodendrimers were prepared via coordination-driven self-assembly. The structures of the newly designed polysulfurated metallodendrimers were characterized by multinuclear NMR ( 1H and 31P), mass spectrometry (CSI-TOF-MS), and elemental analysis. Moreover, the shape and size of these novel metallodendrimers were investigated with PM6 semi-empirical molecular orbital methods.

UR - https://www.scopus.com/pages/publications/84878891126

U2 - 10.1016/j.tet.2013.04.058

DO - 10.1016/j.tet.2013.04.058

M3 - 文章

AN - SCOPUS:84878891126

SN - 0040-4020

VL - 69

SP - 5981

EP - 5988

JO - Tetrahedron

JF - Tetrahedron

IS - 29

ER -

Design and construction of supramolecular polysulfurated metallodendrimers with various shapes and sizes via coordination-driven self-assembly

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