Synthesis, Configurational Analysis, Molecular Recognition and Chirality Sensing of Methylene‐Bridged Naphthotubes

Macrocyclic hosts with a well‐defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene‐bridged naphthotubes, with well‐defined cavities. They were synthesized through TFA‐catalyze...

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Published in:Angewandte Chemie International Edition Vol. 61; no. 42; pp. e202211853 - n/a
Main Authors: Wang, Yan‐Fang, Yao, Huan, Yang, Liu‐Pan, Quan, Mao, Jiang, Wei
Format: Journal Article
Language:English
Published: WEINHEIM Wiley 17.10.2022
Wiley Subscription Services, Inc
Edition:International ed. in English
Subjects:
Alcohols
binding capacity
Cations
Chemical reactions
Chemical synthesis
Chemistry
Chemistry, Multidisciplinary
Chirality
Chirality Sensing
Conformation
Friedel-Crafts reaction
Holes
Homology
Host–Guest Chemistry
Macrocycles
macrocyclic compounds
Methylene
Molecular Conformation
Molecular Recognition
Naphthotubes
optical isomerism
Physical Sciences
Recognition
Science & Technology
Host-Guest Chemistry
BIS-NAPHTHALENE
Naphthotubes
Chirality Sensing
CAVITY
COMPLEXES
Macrocycles
Molecular Recognition
MACROCYCLIC HOSTS
CALIXARENES
FAMILY
ISSN:1433-7851, 1521-3773, 1521-3773
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Abstract Macrocyclic hosts with a well‐defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene‐bridged naphthotubes, with well‐defined cavities. They were synthesized through TFA‐catalyzed Friedel–Crafts reactions between alkoxy‐substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three‐membered macrocycles possess a single cavity, while four‐membered macrocycles adopt a double‐cavity conformation or a self‐filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 108 M−1) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well‐defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms. Methylene‐bridged naphthotubes have been successfully developed. The three‐membered naphthotubes possess a rigid and well‐defined cavity, while four‐membered naphthotubes possess a double‐cavity conformation or a self‐filling conformation depending on the alkoxy length. They show quite strong binding affinities (up to 108 M−1) to organic cations and can be used as chirality sensors for chiral organic cations.
AbstractList Macrocyclic hosts with a well‐defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene‐bridged naphthotubes, with well‐defined cavities. They were synthesized through TFA‐catalyzed Friedel–Crafts reactions between alkoxy‐substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three‐membered macrocycles possess a single cavity, while four‐membered macrocycles adopt a double‐cavity conformation or a self‐filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 108 M−1) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well‐defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms. Methylene‐bridged naphthotubes have been successfully developed. The three‐membered naphthotubes possess a rigid and well‐defined cavity, while four‐membered naphthotubes possess a double‐cavity conformation or a self‐filling conformation depending on the alkoxy length. They show quite strong binding affinities (up to 108 M−1) to organic cations and can be used as chirality sensors for chiral organic cations.
Macrocyclic hosts with a well‐defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene‐bridged naphthotubes, with well‐defined cavities. They were synthesized through TFA‐catalyzed Friedel–Crafts reactions between alkoxy‐substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three‐membered macrocycles possess a single cavity, while four‐membered macrocycles adopt a double‐cavity conformation or a self‐filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 10⁸ M⁻¹) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well‐defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms.
Macrocyclic hosts with a well‐defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene‐bridged naphthotubes, with well‐defined cavities. They were synthesized through TFA‐catalyzed Friedel–Crafts reactions between alkoxy‐substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three‐membered macrocycles possess a single cavity, while four‐membered macrocycles adopt a double‐cavity conformation or a self‐filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 10 8  M −1 ) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well‐defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms.
Macrocyclic hosts with a well‐defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene‐bridged naphthotubes, with well‐defined cavities. They were synthesized through TFA‐catalyzed Friedel–Crafts reactions between alkoxy‐substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three‐membered macrocycles possess a single cavity, while four‐membered macrocycles adopt a double‐cavity conformation or a self‐filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 108 M−1) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well‐defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms.
Macrocyclic hosts with a well-defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene-bridged naphthotubes, with well-defined cavities. They were synthesized through TFA-catalyzed Friedel-Crafts reactions between alkoxy-substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three-membered macrocycles possess a single cavity, while four-membered macrocycles adopt a double-cavity conformation or a self-filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 10(8) M-1) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well-defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms.
Macrocyclic hosts with a well-defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene-bridged naphthotubes, with well-defined cavities. They were synthesized through TFA-catalyzed Friedel-Crafts reactions between alkoxy-substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three-membered macrocycles possess a single cavity, while four-membered macrocycles adopt a double-cavity conformation or a self-filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 108  M-1 ) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well-defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms.Macrocyclic hosts with a well-defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene-bridged naphthotubes, with well-defined cavities. They were synthesized through TFA-catalyzed Friedel-Crafts reactions between alkoxy-substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three-membered macrocycles possess a single cavity, while four-membered macrocycles adopt a double-cavity conformation or a self-filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 108  M-1 ) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well-defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms.
Macrocyclic hosts with a well-defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a new class of macrocyclic hosts, namely methylene-bridged naphthotubes, with well-defined cavities. They were synthesized through TFA-catalyzed Friedel-Crafts reactions between alkoxy-substituted bisnaphthalenes and paraformaldehyde. A configurational selection was observed. Three-membered macrocycles possess a single cavity, while four-membered macrocycles adopt a double-cavity conformation or a self-filling conformation depending on the alkoxy length. The small homologue shows quite strong binding affinities (up to 10  M ) to organic cations, which is better than structurally similar but flexible macrocycles. This demonstrates the advantage of a well-defined cavity in molecular recognition. Moreover, these naphthotubes can be used as chirality sensors for chiral organic cations through different chirality transfer mechanisms.
ArticleNumber 202211853
Author Yang, Liu‐Pan
Quan, Mao
Wang, Yan‐Fang
Jiang, Wei
Yao, Huan
Author_xml – sequence: 1
  givenname: Yan‐Fang
  surname: Wang
  fullname: Wang, Yan‐Fang
  organization: Southern University of Science and Technology
– sequence: 2
  givenname: Huan
  surname: Yao
  fullname: Yao, Huan
  organization: Southern University of Science and Technology
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  givenname: Liu‐Pan
  surname: Yang
  fullname: Yang, Liu‐Pan
  organization: Southern University of Science and Technology
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  givenname: Mao
  surname: Quan
  fullname: Quan, Mao
  email: quanm@sustech.edu.cn
  organization: Southern University of Science and Technology
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  givenname: Wei
  orcidid: 0000-0001-7683-5811
  surname: Jiang
  fullname: Jiang, Wei
  email: jiangw@sustech.edu.cn
  organization: Southern University of Science and Technology
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Issue 42
Keywords Host-Guest Chemistry
BIS-NAPHTHALENE
Naphthotubes
Chirality Sensing
CAVITY
COMPLEXES
Macrocycles
Molecular Recognition
MACROCYCLIC HOSTS
CALIXARENES
FAMILY
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PublicationTitle Angewandte Chemie International Edition
PublicationTitleAbbrev ANGEW CHEM INT EDIT
PublicationTitleAlternate Angew Chem Int Ed Engl
PublicationYear 2022
Publisher Wiley
Wiley Subscription Services, Inc
Publisher_xml – name: Wiley
– name: Wiley Subscription Services, Inc
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Snippet Macrocyclic hosts with a well‐defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a...
Macrocyclic hosts with a well-defined cavity are particularly appealing for supramolecular chemistry, but they are still rare. In this research, we reported a...
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StartPage e202211853
SubjectTerms Alcohols
binding capacity
Cations
Chemical reactions
Chemical synthesis
Chemistry
Chemistry, Multidisciplinary
Chirality
Chirality Sensing
Conformation
Friedel-Crafts reaction
Holes
Homology
Host–Guest Chemistry
Macrocycles
macrocyclic compounds
Methylene
Molecular Conformation
Molecular Recognition
Naphthotubes
optical isomerism
Physical Sciences
Recognition
Science & Technology
Title Synthesis, Configurational Analysis, Molecular Recognition and Chirality Sensing of Methylene‐Bridged Naphthotubes
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202211853
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https://www.ncbi.nlm.nih.gov/pubmed/36042003
https://www.proquest.com/docview/2723275097
https://www.proquest.com/docview/2708735120
https://www.proquest.com/docview/2811989053
Volume 61
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