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Structure-activity strategies for mechanically responsive fluorescent materials: a molecular perspective
Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation. Usually, MRL can be regulated by intermolecular interactions, molecular conformation or molecular packing, to achieve the desirable optical properties. Herein, at the molecular level, t...
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Published in: | Chemical communications (Cambridge, England) England), 2023-12, Vol.6 (1), p.1-25 |
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creator | Fei, Guiqiang Li, Shaoqi Liu, Yuxia Carney, Jared B Chen, Tao Li, Yulin Gao, Xiaoyong Chen, Ji Chen, Pu Yue, Yanfeng Bao, Kai Tang, Bo Chen, Guang |
description | Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation. Usually, MRL can be regulated by intermolecular interactions, molecular conformation or molecular packing, to achieve the desirable optical properties. Herein, at the molecular level, this review covers the factors that influence mechanically responsive fluorescent materials, involving the single- or multifactorial modulation of aliphatic chains, donor-receptor switch, substituent adjustment, and position isomerism. According to these factors, the structure-activity strategies can be summarized as: (i) the self-recovery of optical properties, from the final to initial state, can be regulated by introducing long alkyl chains to a fluorophore. (ii) The sensitivity of MRL materials can be controlled by modifying the donor-acceptor structure
via
the changed ICT (intramolecular charge transfer) and intramolecular interaction. (iii) The electronic and steric effects of substituents can affect ICT and intermolecular interactions, thereby resulting in high quantum yield and high-contrast MRL materials
via
changing the molecular stacking of crystalline states. (iv) Intermolecular interaction is modulated by the position isomerism of the substituents, which results in switched molecular packing for the extended response toward a wide range of stimuli. It is anticipated that the molecular mechanisms of these structure-activity relationships will serve as a significant reference for developing novel, high contrast, recyclable mechanical response luminous materials.
Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation. |
doi_str_mv | 10.1039/d3cc04992b |
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via
the changed ICT (intramolecular charge transfer) and intramolecular interaction. (iii) The electronic and steric effects of substituents can affect ICT and intermolecular interactions, thereby resulting in high quantum yield and high-contrast MRL materials
via
changing the molecular stacking of crystalline states. (iv) Intermolecular interaction is modulated by the position isomerism of the substituents, which results in switched molecular packing for the extended response toward a wide range of stimuli. It is anticipated that the molecular mechanisms of these structure-activity relationships will serve as a significant reference for developing novel, high contrast, recyclable mechanical response luminous materials.
Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d3cc04992b</identifier><identifier>PMID: 38018176</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Charge transfer ; Fluorescence ; Mechanical analysis ; Molecular chains ; Molecular conformation ; Molecular structure ; Optical properties ; Steric effects</subject><ispartof>Chemical communications (Cambridge, England), 2023-12, Vol.6 (1), p.1-25</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-fc90ca14b684cc74681636e095320e2d9b19830eb04aec3602c2af94bb0063a63</citedby><cites>FETCH-LOGICAL-c373t-fc90ca14b684cc74681636e095320e2d9b19830eb04aec3602c2af94bb0063a63</cites><orcidid>0000-0003-1139-8563 ; 0000-0002-8712-7025 ; 0000-0002-0214-1806 ; 0000-0002-0454-1686</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38018176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fei, Guiqiang</creatorcontrib><creatorcontrib>Li, Shaoqi</creatorcontrib><creatorcontrib>Liu, Yuxia</creatorcontrib><creatorcontrib>Carney, Jared B</creatorcontrib><creatorcontrib>Chen, Tao</creatorcontrib><creatorcontrib>Li, Yulin</creatorcontrib><creatorcontrib>Gao, Xiaoyong</creatorcontrib><creatorcontrib>Chen, Ji</creatorcontrib><creatorcontrib>Chen, Pu</creatorcontrib><creatorcontrib>Yue, Yanfeng</creatorcontrib><creatorcontrib>Bao, Kai</creatorcontrib><creatorcontrib>Tang, Bo</creatorcontrib><creatorcontrib>Chen, Guang</creatorcontrib><title>Structure-activity strategies for mechanically responsive fluorescent materials: a molecular perspective</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation. Usually, MRL can be regulated by intermolecular interactions, molecular conformation or molecular packing, to achieve the desirable optical properties. Herein, at the molecular level, this review covers the factors that influence mechanically responsive fluorescent materials, involving the single- or multifactorial modulation of aliphatic chains, donor-receptor switch, substituent adjustment, and position isomerism. According to these factors, the structure-activity strategies can be summarized as: (i) the self-recovery of optical properties, from the final to initial state, can be regulated by introducing long alkyl chains to a fluorophore. (ii) The sensitivity of MRL materials can be controlled by modifying the donor-acceptor structure
via
the changed ICT (intramolecular charge transfer) and intramolecular interaction. (iii) The electronic and steric effects of substituents can affect ICT and intermolecular interactions, thereby resulting in high quantum yield and high-contrast MRL materials
via
changing the molecular stacking of crystalline states. (iv) Intermolecular interaction is modulated by the position isomerism of the substituents, which results in switched molecular packing for the extended response toward a wide range of stimuli. It is anticipated that the molecular mechanisms of these structure-activity relationships will serve as a significant reference for developing novel, high contrast, recyclable mechanical response luminous materials.
Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation.</description><subject>Charge transfer</subject><subject>Fluorescence</subject><subject>Mechanical analysis</subject><subject>Molecular chains</subject><subject>Molecular conformation</subject><subject>Molecular structure</subject><subject>Optical properties</subject><subject>Steric effects</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkd2rEzEQxYMotlZffL-XgC8irCaZbLq5b7p-QsEHFXxbstNZu2W_bpIt9L83tbWC85IJ88uZwwljz6V4LQXYN1tAFNpaVT9gSwlGZ7kufj489bnN1qDzBXsSwl6kknnxmC2gELKQa7Nku2_RzxhnT5nD2B7aeOQhehfpV0uBN6PnPeHODS26rjtyT2Eah9AeiDfdPKYr0hB5nx741nXhjjvejx3h3DnPJ_JhopMuPWWPmjSnZ5dzxX58_PC9_Jxtvn76Ur7dZAhriFmDVqCTujaFRlxrU0gDhoTNQQlSW1tLW4CgWmhHCEYoVK6xuq6FMOAMrNjLs-7kx_uZQqz6NnnsOjfQOIdKFTZXRgDohL74D92Psx-Su0rZRIhcprUr9upMoR9D8NRUk29754-VFNUp_-o9lOWf_N8l-PYiOdc9ba_o38ATcHMGfMDr9N8Hwm-zyYty</recordid><startdate>20231219</startdate><enddate>20231219</enddate><creator>Fei, Guiqiang</creator><creator>Li, Shaoqi</creator><creator>Liu, Yuxia</creator><creator>Carney, Jared B</creator><creator>Chen, Tao</creator><creator>Li, Yulin</creator><creator>Gao, Xiaoyong</creator><creator>Chen, Ji</creator><creator>Chen, Pu</creator><creator>Yue, Yanfeng</creator><creator>Bao, Kai</creator><creator>Tang, Bo</creator><creator>Chen, Guang</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1139-8563</orcidid><orcidid>https://orcid.org/0000-0002-8712-7025</orcidid><orcidid>https://orcid.org/0000-0002-0214-1806</orcidid><orcidid>https://orcid.org/0000-0002-0454-1686</orcidid></search><sort><creationdate>20231219</creationdate><title>Structure-activity strategies for mechanically responsive fluorescent materials: a molecular perspective</title><author>Fei, Guiqiang ; Li, Shaoqi ; Liu, Yuxia ; Carney, Jared B ; Chen, Tao ; Li, Yulin ; Gao, Xiaoyong ; Chen, Ji ; Chen, Pu ; Yue, Yanfeng ; Bao, Kai ; Tang, Bo ; Chen, Guang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-fc90ca14b684cc74681636e095320e2d9b19830eb04aec3602c2af94bb0063a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Charge transfer</topic><topic>Fluorescence</topic><topic>Mechanical analysis</topic><topic>Molecular chains</topic><topic>Molecular conformation</topic><topic>Molecular structure</topic><topic>Optical properties</topic><topic>Steric effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fei, Guiqiang</creatorcontrib><creatorcontrib>Li, Shaoqi</creatorcontrib><creatorcontrib>Liu, Yuxia</creatorcontrib><creatorcontrib>Carney, Jared B</creatorcontrib><creatorcontrib>Chen, Tao</creatorcontrib><creatorcontrib>Li, Yulin</creatorcontrib><creatorcontrib>Gao, Xiaoyong</creatorcontrib><creatorcontrib>Chen, Ji</creatorcontrib><creatorcontrib>Chen, Pu</creatorcontrib><creatorcontrib>Yue, Yanfeng</creatorcontrib><creatorcontrib>Bao, Kai</creatorcontrib><creatorcontrib>Tang, Bo</creatorcontrib><creatorcontrib>Chen, Guang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fei, Guiqiang</au><au>Li, Shaoqi</au><au>Liu, Yuxia</au><au>Carney, Jared B</au><au>Chen, Tao</au><au>Li, Yulin</au><au>Gao, Xiaoyong</au><au>Chen, Ji</au><au>Chen, Pu</au><au>Yue, Yanfeng</au><au>Bao, Kai</au><au>Tang, Bo</au><au>Chen, Guang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure-activity strategies for mechanically responsive fluorescent materials: a molecular perspective</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2023-12-19</date><risdate>2023</risdate><volume>6</volume><issue>1</issue><spage>1</spage><epage>25</epage><pages>1-25</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation. Usually, MRL can be regulated by intermolecular interactions, molecular conformation or molecular packing, to achieve the desirable optical properties. Herein, at the molecular level, this review covers the factors that influence mechanically responsive fluorescent materials, involving the single- or multifactorial modulation of aliphatic chains, donor-receptor switch, substituent adjustment, and position isomerism. According to these factors, the structure-activity strategies can be summarized as: (i) the self-recovery of optical properties, from the final to initial state, can be regulated by introducing long alkyl chains to a fluorophore. (ii) The sensitivity of MRL materials can be controlled by modifying the donor-acceptor structure
via
the changed ICT (intramolecular charge transfer) and intramolecular interaction. (iii) The electronic and steric effects of substituents can affect ICT and intermolecular interactions, thereby resulting in high quantum yield and high-contrast MRL materials
via
changing the molecular stacking of crystalline states. (iv) Intermolecular interaction is modulated by the position isomerism of the substituents, which results in switched molecular packing for the extended response toward a wide range of stimuli. It is anticipated that the molecular mechanisms of these structure-activity relationships will serve as a significant reference for developing novel, high contrast, recyclable mechanical response luminous materials.
Mechanical response luminescence (MRL) describes the photophysical properties triggered by mechanical stimulation.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38018176</pmid><doi>10.1039/d3cc04992b</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-1139-8563</orcidid><orcidid>https://orcid.org/0000-0002-8712-7025</orcidid><orcidid>https://orcid.org/0000-0002-0214-1806</orcidid><orcidid>https://orcid.org/0000-0002-0454-1686</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Charge transfer Fluorescence Mechanical analysis Molecular chains Molecular conformation Molecular structure Optical properties Steric effects |
title | Structure-activity strategies for mechanically responsive fluorescent materials: a molecular perspective |
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