Literature DB >> 18815679

Heterocalixaromatics, new generation macrocyclic host molecules in supramolecular chemistry.

Mei-Xiang Wang1.   

Abstract

Heterocalixaromatics, the heteroatom bridged calix(hetero)arenes, have been emerging as new generation macrocyclic host molecules in supramolecular chemistry recently. Being different from the conventional calixarenes in which the aromatic rings are linked by methylene units, heterocalixaromatics assemble various aromatic rings by different heteroatoms. Owning to the intrinsic nature of heteroatoms that can adopt different electronic configurations to form various degrees of conjugation with their neighboring aromatic rings, heterocalixaromatics exhibit unique structural features and versatile recognition properties in comparison to conventional calixarenes. This feature article highlights recent advances in the synthesis, functionalization, structure and molecular recognition of nitrogen- and/or oxygen-bridged calixaromatics, with a primary focus on our own work.

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Year:  2008        PMID: 18815679     DOI: 10.1039/b809287g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  10 in total

1.  Air-oxidation from sulfur to sulfone-bridged Schiff-base macrocyclic complexes showing enhanced antimicrobial activities.

Authors:  Genfeng Feng; Yunshan Shi; Lei Zhang; Rongguang Shi; Wei Huang; Ruiyong Wang
Journal:  Sci Rep       Date:  2017-11-21       Impact factor: 4.379

2.  Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening.

Authors:  Jia Shang; Brett M Rambo; Xiang Hao; Jun-Feng Xiang; Han-Yuan Gong; Jonathan L Sessler
Journal:  Chem Sci       Date:  2016-03-09       Impact factor: 9.825

Review 3.  Gene delivery based on macrocyclic amphiphiles.

Authors:  Wen-Chao Geng; Qiaoxian Huang; Zhe Xu; Ruibing Wang; Dong-Sheng Guo
Journal:  Theranostics       Date:  2019-05-18       Impact factor: 11.556

4.  Complexation of a guanidinium-modified calixarene with diverse dyes and investigation of the corresponding photophysical response.

Authors:  Yu-Ying Wang; Yong Kong; Zhe Zheng; Wen-Chao Geng; Zi-Yi Zhao; Hongwei Sun; Dong-Sheng Guo
Journal:  Beilstein J Org Chem       Date:  2019-06-25       Impact factor: 2.883

5.  Covalent Organic Framework Based on Azacalix[4]arene for the Efficient Capture of Dialysis Waste Products.

Authors:  Tina Skorjanc; Dinesh Shetty; Felipe Gándara; Simon Pascal; Nawavi Naleem; Salma Abubakar; Liaqat Ali; Abdul Khayum Mohammed; Jesus Raya; Serdal Kirmizialtin; Olivier Siri; Ali Trabolsi
Journal:  ACS Appl Mater Interfaces       Date:  2022-08-22       Impact factor: 10.383

6.  Hexathioalkyl sumanenes: an electron-donating buckybowl as a building block for supramolecular materials.

Authors:  Yoshiaki Shoji; Takashi Kajitani; Fumitaka Ishiwari; Qiang Ding; Hiroyasu Sato; Hayato Anetai; Tomoyuki Akutagawa; Hidehiro Sakurai; Takanori Fukushima
Journal:  Chem Sci       Date:  2017-10-18       Impact factor: 9.825

7.  Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities.

Authors:  Fei Jia; Zhenfeng He; Liu-Pan Yang; Zhi-Sheng Pan; Min Yi; Ren-Wang Jiang; Wei Jiang
Journal:  Chem Sci       Date:  2015-09-14       Impact factor: 9.825

8.  Synthesis and post-functionalization of alternate-linked-meta-para-[2 n .1 n ]thiacyclophanes.

Authors:  Wout De Leger; Koen Adriaensen; Koen Robeyns; Luc Van Meervelt; Joice Thomas; Björn Meijers; Mario Smet; Wim Dehaen
Journal:  Beilstein J Org Chem       Date:  2018-08-22       Impact factor: 2.883

9.  Synthesis and anion binding properties of phthalimide-containing corona[6]arenes.

Authors:  Meng-Di Gu; Yao Lu; Mei-Xiang Wang
Journal:  Beilstein J Org Chem       Date:  2019-08-21       Impact factor: 2.883

10.  Synthesis of a novel aminobenzene-containing hemicucurbituril and its fluorescence spectral properties with ions.

Authors:  Qingkai Zeng; Qiumeng Long; Jihong Lu; Li Wang; Yuting You; Xiaoting Yuan; Qianjun Zhang; Qingmei Ge; Hang Cong; Mao Liu
Journal:  Beilstein J Org Chem       Date:  2021-12-06       Impact factor: 2.883

  10 in total

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