Literature DB >> 26477517

Helix Sense-Selective Supramolecular Polymerization Seeded by a One-Handed Helical Polymeric Assembly.

Wei Zhang1,2, Wusong Jin3, Takanori Fukushima4, Tadashi Mori5, Takuzo Aida1,2.   

Abstract

Helix sense-selective supramolecular polymerization was achieved using a one-handed helical nanotubular polymeric assembly as a seed. First, bipyridine (BPY)-appended achiral hexabenzocoronene ((BPY)HBC) was copolymerized noncovalently with chiral (BPY)HBC(S) (or (BPY)HBC(R)) at a molar ratio of 9:1, which, via the sergeants-and-soldiers effect, afforded a P-helical (or M-helical) nanotube, which was then treated with Cu(2+) to transform into structurally robust ((BPY)Cu)NT(P) (or ((BPY)Cu)NT(M)) with a Cu(2+)/BPY coordination polymer shell. Helical seeds ((BPY)Cu)NT(P) and ((BPY)Cu)NT(M) brought about the controlled assembly of fluorinated chiral FHBC(S) and FHBC(R) as well as achiral FHBC to yield one-handed helical nanotubular supramolecular block copolymers, in which the helical senses of the newly formed block segments were solely determined by those of the helical seeds employed. Noteworthy, FHBC(S) and FHBC(R) alone without the helical seeds form ill-defined agglomerates. Attempted supramolecular polymerization of a racemic mixture of FHBC(S) and FHBC(R) from ((BPY)Cu)NT(P) (or ((BPY)Cu)NT(M)) resulted in its chiral separation, affording P-helical (or M-helical) diastereomeric block segments composed of FHBC(S)and FHBC(R) with different thermodynamic properties.

Entities:  

Year:  2015        PMID: 26477517     DOI: 10.1021/jacs.5b09878

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  7 in total

Review 1.  Diels-Alder Cycloaddition with CO, CO2, SO2, or N2 Extrusion: A Powerful Tool for Material Chemistry.

Authors:  Stanisław Krompiec; Aneta Kurpanik-Wójcik; Marek Matussek; Bogumiła Gołek; Angelika Mieszczanin; Aleksandra Fijołek
Journal:  Materials (Basel)       Date:  2021-12-27       Impact factor: 3.623

2.  Synthesis of highly substituted benzene ring systems through three-component coupling of enyne imines, Fischer carbene complexes, and electron-deficient alkynes.

Authors:  Bishnu Dhakal; Lalith S R Gamage; Yanshi Zhang; James W Herndon
Journal:  Tetrahedron Lett       Date:  2017-02-24       Impact factor: 2.415

3.  Oriented arrangement of simple monomers enabled by confinement: towards living supramolecular polymerization.

Authors:  Yingtong Zong; Si-Min Xu; Wenying Shi; Chao Lu
Journal:  Nat Commun       Date:  2021-05-10       Impact factor: 14.919

4.  Supramolecular Copolymers: Structure and Composition Revealed by Theoretical Modeling.

Authors:  Anindita Das; Ghislaine Vantomme; Albert J Markvoort; Huub M M Ten Eikelder; Miguel Garcia-Iglesias; Anja R A Palmans; E W Meijer
Journal:  J Am Chem Soc       Date:  2017-05-16       Impact factor: 15.419

5.  Steric ploy for alternating donor-acceptor co-assembly and cooperative supramolecular polymerization.

Authors:  Saptarshi Chakraborty; Haridas Kar; Amrita Sikder; Suhrit Ghosh
Journal:  Chem Sci       Date:  2016-09-19       Impact factor: 9.825

6.  Unraveling Mechanisms of Chiral Induction in Double-Helical Metallopolymers.

Authors:  Jake L Greenfield; Emrys W Evans; Daniele Di Nuzzo; Marco Di Antonio; Richard H Friend; Jonathan R Nitschke
Journal:  J Am Chem Soc       Date:  2018-08-01       Impact factor: 15.419

7.  Supramolecular polymerization of electronically complementary linear motifs: anti-cooperativity by attenuated growth.

Authors:  Yeray Dorca; Cristina Naranjo; Goutam Ghosh; Bartolomé Soberats; Joaquín Calbo; Enrique Ortí; Gustavo Fernández; Luis Sánchez
Journal:  Chem Sci       Date:  2021-11-03       Impact factor: 9.825

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.