A chiral spirobifluorene-based bis(salen) zinc(ii) receptor towards highly enantioselective binding of chiral carboxylates-Reference-Cited by-同舟云学术

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A chiral spirobifluorene-based bis(salen) zinc(ii) receptor towards highly enantioselective binding of chiral carboxylates

Published:2021 Issue:12 Volume:50 Page:4119-4123
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Ikbal Sk Asif¹²³⁴,Sakata Yoko¹²³⁴⁵^ORCID,Akine Shigehisa¹²³⁴⁵^ORCID

Affiliation:

1. Nano Life Science Institute (WPI-NanoLSI)

2. Kanazawa University

3. Kanazawa 920-1192

4. Japan

5. Graduate School of Natural Science and Technology

Abstract

A new chiral receptor based on two salen zinc(ii) complex units and a spirobifluorene linker enantioselectively binds chiral carboxylate guests.

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/DT/D1DT00218J

Reference65 articles.

1. Synthetic receptors for carboxylic acids and carboxylates

2. Recognition of Chiral Carboxylic Anions by Artificial Receptors

3. Complexation and sensing of dicarboxylate anions and dicarboxylic acids

4. Rapid Optical Methods for Enantiomeric Excess Analysis: From Enantioselective Indicator Displacement Assays to Exciton-Coupled Circular Dichroism

5. Anion receptors based on organic frameworks: highlights from 2005 and 2006

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1. Lewis Acidic Zinc(II) Complexes of Tetradentate Ligands as Building Blocks for Responsive Assembled Supramolecular Structures;Chemistry;2023-01-13

2. Enantiomers Identification of Penicillamine by Chiral Mono-Schiff Base Macrocycles;Acta Chimica Sinica;2023

3. Spirobifluorene derivatives and their biomaterial applications: Current trends;Journal of Molecular Structure;2022-05

4. Lewis acidic zinc(ii) salen-type Schiff-base complexes: sensing properties and responsive nanostructures;Dalton Transactions;2021

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