Self-assembly of hydrazide-based heterodimers driven by hydrogen bonding and donor-acceptor interaction

Dai Jun Feng; Peng Wang; Xiao Qiang Li; Zhan Ting Li

doi:10.1002/cjoc.200690224

Self-assembly of hydrazide-based heterodimers driven by hydrogen bonding and donor-acceptor interaction

Dai Jun Feng
, Peng Wang
, Xiao Qiang Li
, Zhan Ting Li

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Abstract

A new series of hydrogen bonding-driven heterodimers have been self-assembled in chloroform from hydrazide-based monomers. Additional intermolecular donor-acceptor interaction between the electron-rich bis(p-phenylene)-34-crown-10 unit and the electron-deficient naphthalene diimide unit has been utilized to increase the stability of the dimmers, and pronounced cooperativity of the two discrete non-covalent forces to stabilize the dimer has been revealed by the quantitative ¹H (2D) NMR and UV-Vis experiments.

Original language	English
Pages (from-to)	1200-1208
Number of pages	9
Journal	Chinese Journal of Chemistry
Volume	24
Issue number	9
DOIs	https://doi.org/10.1002/cjoc.200690224
State	Published - Sep 2006
Externally published	Yes

Keywords

Donor-acceptor interaction
Heterodimer
Hydrazide
Hydrogen bonding
Self-assembly

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10.1002/cjoc.200690224

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title = "Self-assembly of hydrazide-based heterodimers driven by hydrogen bonding and donor-acceptor interaction",

abstract = "A new series of hydrogen bonding-driven heterodimers have been self-assembled in chloroform from hydrazide-based monomers. Additional intermolecular donor-acceptor interaction between the electron-rich bis(p-phenylene)-34-crown-10 unit and the electron-deficient naphthalene diimide unit has been utilized to increase the stability of the dimmers, and pronounced cooperativity of the two discrete non-covalent forces to stabilize the dimer has been revealed by the quantitative 1H (2D) NMR and UV-Vis experiments.",

keywords = "Donor-acceptor interaction, Heterodimer, Hydrazide, Hydrogen bonding, Self-assembly",

author = "Feng, \{Dai Jun\} and Peng Wang and Li, \{Xiao Qiang\} and Li, \{Zhan Ting\}",

year = "2006",

month = sep,

doi = "10.1002/cjoc.200690224",

language = "English",

volume = "24",

pages = "1200--1208",

journal = "Chinese Journal of Chemistry",

issn = "1001-604X",

publisher = "John Wiley and Sons Inc.",

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TY - JOUR

T1 - Self-assembly of hydrazide-based heterodimers driven by hydrogen bonding and donor-acceptor interaction

AU - Feng, Dai Jun

AU - Wang, Peng

AU - Li, Xiao Qiang

AU - Li, Zhan Ting

PY - 2006/9

Y1 - 2006/9

N2 - A new series of hydrogen bonding-driven heterodimers have been self-assembled in chloroform from hydrazide-based monomers. Additional intermolecular donor-acceptor interaction between the electron-rich bis(p-phenylene)-34-crown-10 unit and the electron-deficient naphthalene diimide unit has been utilized to increase the stability of the dimmers, and pronounced cooperativity of the two discrete non-covalent forces to stabilize the dimer has been revealed by the quantitative 1H (2D) NMR and UV-Vis experiments.

AB - A new series of hydrogen bonding-driven heterodimers have been self-assembled in chloroform from hydrazide-based monomers. Additional intermolecular donor-acceptor interaction between the electron-rich bis(p-phenylene)-34-crown-10 unit and the electron-deficient naphthalene diimide unit has been utilized to increase the stability of the dimmers, and pronounced cooperativity of the two discrete non-covalent forces to stabilize the dimer has been revealed by the quantitative 1H (2D) NMR and UV-Vis experiments.

KW - Donor-acceptor interaction

KW - Heterodimer

KW - Hydrazide

KW - Hydrogen bonding

KW - Self-assembly

UR - https://www.scopus.com/pages/publications/33750060082

U2 - 10.1002/cjoc.200690224

DO - 10.1002/cjoc.200690224

M3 - Article

AN - SCOPUS:33750060082

SN - 1001-604X

VL - 24

SP - 1200

EP - 1208

JO - Chinese Journal of Chemistry

JF - Chinese Journal of Chemistry

IS - 9

ER -

Self-assembly of hydrazide-based heterodimers driven by hydrogen bonding and donor-acceptor interaction

Abstract

Keywords

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