Multi-functional ion-sensor based on a photochromic diarylethene with a 1H-imidazo [4,5-f][1,10] phenanthroline unit

A new asymmetrical diarylethene containing a 1H‐imidazo [4,5‐f][1,10] phenanthroline unit was synthesized. The compound showed typical photochromism and functioned as a notable fluorescence switch upon alternating irradiation with ultraviolet (UV) and visible light. Its closed‐ring isomer could be u...

Full description

Saved in:
Bibliographic Details
Published in:Luminescence (Chichester, England) England), 2015-12, Vol.30 (8), p.1290-1296
Main Authors: Wang, Renjie, Dong, Xiaorong, Liu, Gang, Ren, Panpan, Pu, Shouzhi
Format: Article
Language:English
Subjects:
Asymmetry
cation recognition
Color
diarylethene
Ethylenes - chemistry
Fluorescence
Fluorescent Dyes - chemical synthesis
Fluorescent Dyes - chemistry
imidazole-containing substituent
Isomers
logic circuit
Luminescence
Luminous intensity
Molecular Structure
Phenanthrolines - chemistry
photochromism
Spectrometry, Fluorescence
Stimuli
Switches
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 1296
container_issue 8
container_start_page 1290
container_title Luminescence (Chichester, England)
container_volume 30
creator Wang, Renjie
Dong, Xiaorong
Liu, Gang
Ren, Panpan
Pu, Shouzhi
description A new asymmetrical diarylethene containing a 1H‐imidazo [4,5‐f][1,10] phenanthroline unit was synthesized. The compound showed typical photochromism and functioned as a notable fluorescence switch upon alternating irradiation with ultraviolet (UV) and visible light. Its closed‐ring isomer could be used as a selective ‘naked‐eye’ colorimetric sensor for Cu2+, accompanied by a notable color change from blue to colorless. Furthermore, the compound was found to be selective towards Ca2+, Mg2+, and Sr2+ with significant fluorescence changes. On the basis of this characteristic, a logic circuit was constructed by utilizing both light and chemical stimuli as inputs and fluorescence intensity at 487 nm as output. Copyright © 2015 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/bio.2895
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1800483460</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1800483460</sourcerecordid><originalsourceid>FETCH-LOGICAL-i4185-df46a3fbe0dee1728096c27ccd368be56278db346417c46e3627c22b28d79ae03</originalsourceid><addsrcrecordid>eNqN0c9rFDEUB_AgFlur4F8gA148NDW_kznaVbuFraVQ8VBKyGTesKkzk3WSoda_vllaV_DkJS8kn_cO34fQG0qOKSHsQxPiMTO1fIYOqGQMayb4892dy330MqVbQohSqn6B9pk0QlOmDlA-n_sccDePPoc4ur4qJ04wpjhVjUvQVnGsXLVZxxz9eopD8FUb3HTfQ17DCNVdyOsC6BKHIbTud6yuxZHE3c01PaLkpnTC6MZcWvtQ-DyG_Artda5P8PqpHqJvXz5fLZZ4dXF6tvi4wkFQI3HbCeV41wBpAahmhtTKM-19y5VpQCqmTdtwoQTVXijg5cEz1jDT6toB4Yfo_ePczRR_zpCyHULy0PduhDgnSw0hwpQB_0G1IjUzjIhC3_1Db-M8lei2SmpKlZSqqLdPam4GaO1mCkNJzf6JvgD8CO5CD_e7f0rsdqW2rNRuV2pPzi629a8PKcOvnXfTD6s019J-_3pqV58uF0t9vrKGPwD5KKA7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1757116556</pqid></control><display><type>article</type><title>Multi-functional ion-sensor based on a photochromic diarylethene with a 1H-imidazo [4,5-f][1,10] phenanthroline unit</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Wang, Renjie ; Dong, Xiaorong ; Liu, Gang ; Ren, Panpan ; Pu, Shouzhi</creator><creatorcontrib>Wang, Renjie ; Dong, Xiaorong ; Liu, Gang ; Ren, Panpan ; Pu, Shouzhi</creatorcontrib><description>A new asymmetrical diarylethene containing a 1H‐imidazo [4,5‐f][1,10] phenanthroline unit was synthesized. The compound showed typical photochromism and functioned as a notable fluorescence switch upon alternating irradiation with ultraviolet (UV) and visible light. Its closed‐ring isomer could be used as a selective ‘naked‐eye’ colorimetric sensor for Cu2+, accompanied by a notable color change from blue to colorless. Furthermore, the compound was found to be selective towards Ca2+, Mg2+, and Sr2+ with significant fluorescence changes. On the basis of this characteristic, a logic circuit was constructed by utilizing both light and chemical stimuli as inputs and fluorescence intensity at 487 nm as output. Copyright © 2015 John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 1522-7235</identifier><identifier>EISSN: 1522-7243</identifier><identifier>DOI: 10.1002/bio.2895</identifier><identifier>PMID: 25847126</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Asymmetry ; cation recognition ; Color ; diarylethene ; Ethylenes - chemistry ; Fluorescence ; Fluorescent Dyes - chemical synthesis ; Fluorescent Dyes - chemistry ; imidazole-containing substituent ; Isomers ; logic circuit ; Luminescence ; Luminous intensity ; Molecular Structure ; Phenanthrolines - chemistry ; photochromism ; Spectrometry, Fluorescence ; Stimuli ; Switches</subject><ispartof>Luminescence (Chichester, England), 2015-12, Vol.30 (8), p.1290-1296</ispartof><rights>Copyright © 2015 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/25847126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Renjie</creatorcontrib><creatorcontrib>Dong, Xiaorong</creatorcontrib><creatorcontrib>Liu, Gang</creatorcontrib><creatorcontrib>Ren, Panpan</creatorcontrib><creatorcontrib>Pu, Shouzhi</creatorcontrib><title>Multi-functional ion-sensor based on a photochromic diarylethene with a 1H-imidazo [4,5-f][1,10] phenanthroline unit</title><title>Luminescence (Chichester, England)</title><addtitle>Luminescence</addtitle><description>A new asymmetrical diarylethene containing a 1H‐imidazo [4,5‐f][1,10] phenanthroline unit was synthesized. The compound showed typical photochromism and functioned as a notable fluorescence switch upon alternating irradiation with ultraviolet (UV) and visible light. Its closed‐ring isomer could be used as a selective ‘naked‐eye’ colorimetric sensor for Cu2+, accompanied by a notable color change from blue to colorless. Furthermore, the compound was found to be selective towards Ca2+, Mg2+, and Sr2+ with significant fluorescence changes. On the basis of this characteristic, a logic circuit was constructed by utilizing both light and chemical stimuli as inputs and fluorescence intensity at 487 nm as output. Copyright © 2015 John Wiley &amp; Sons, Ltd.</description><subject>Asymmetry</subject><subject>cation recognition</subject><subject>Color</subject><subject>diarylethene</subject><subject>Ethylenes - chemistry</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - chemical synthesis</subject><subject>Fluorescent Dyes - chemistry</subject><subject>imidazole-containing substituent</subject><subject>Isomers</subject><subject>logic circuit</subject><subject>Luminescence</subject><subject>Luminous intensity</subject><subject>Molecular Structure</subject><subject>Phenanthrolines - chemistry</subject><subject>photochromism</subject><subject>Spectrometry, Fluorescence</subject><subject>Stimuli</subject><subject>Switches</subject><issn>1522-7235</issn><issn>1522-7243</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqN0c9rFDEUB_AgFlur4F8gA148NDW_kznaVbuFraVQ8VBKyGTesKkzk3WSoda_vllaV_DkJS8kn_cO34fQG0qOKSHsQxPiMTO1fIYOqGQMayb4892dy330MqVbQohSqn6B9pk0QlOmDlA-n_sccDePPoc4ur4qJ04wpjhVjUvQVnGsXLVZxxz9eopD8FUb3HTfQ17DCNVdyOsC6BKHIbTud6yuxZHE3c01PaLkpnTC6MZcWvtQ-DyG_Artda5P8PqpHqJvXz5fLZZ4dXF6tvi4wkFQI3HbCeV41wBpAahmhtTKM-19y5VpQCqmTdtwoQTVXijg5cEz1jDT6toB4Yfo_ePczRR_zpCyHULy0PduhDgnSw0hwpQB_0G1IjUzjIhC3_1Db-M8lei2SmpKlZSqqLdPam4GaO1mCkNJzf6JvgD8CO5CD_e7f0rsdqW2rNRuV2pPzi629a8PKcOvnXfTD6s019J-_3pqV58uF0t9vrKGPwD5KKA7</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Wang, Renjie</creator><creator>Dong, Xiaorong</creator><creator>Liu, Gang</creator><creator>Ren, Panpan</creator><creator>Pu, Shouzhi</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H95</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L.G</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201512</creationdate><title>Multi-functional ion-sensor based on a photochromic diarylethene with a 1H-imidazo [4,5-f][1,10] phenanthroline unit</title><author>Wang, Renjie ; Dong, Xiaorong ; Liu, Gang ; Ren, Panpan ; Pu, Shouzhi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i4185-df46a3fbe0dee1728096c27ccd368be56278db346417c46e3627c22b28d79ae03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Asymmetry</topic><topic>cation recognition</topic><topic>Color</topic><topic>diarylethene</topic><topic>Ethylenes - chemistry</topic><topic>Fluorescence</topic><topic>Fluorescent Dyes - chemical synthesis</topic><topic>Fluorescent Dyes - chemistry</topic><topic>imidazole-containing substituent</topic><topic>Isomers</topic><topic>logic circuit</topic><topic>Luminescence</topic><topic>Luminous intensity</topic><topic>Molecular Structure</topic><topic>Phenanthrolines - chemistry</topic><topic>photochromism</topic><topic>Spectrometry, Fluorescence</topic><topic>Stimuli</topic><topic>Switches</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Renjie</creatorcontrib><creatorcontrib>Dong, Xiaorong</creatorcontrib><creatorcontrib>Liu, Gang</creatorcontrib><creatorcontrib>Ren, Panpan</creatorcontrib><creatorcontrib>Pu, Shouzhi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Luminescence (Chichester, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Renjie</au><au>Dong, Xiaorong</au><au>Liu, Gang</au><au>Ren, Panpan</au><au>Pu, Shouzhi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multi-functional ion-sensor based on a photochromic diarylethene with a 1H-imidazo [4,5-f][1,10] phenanthroline unit</atitle><jtitle>Luminescence (Chichester, England)</jtitle><addtitle>Luminescence</addtitle><date>2015-12</date><risdate>2015</risdate><volume>30</volume><issue>8</issue><spage>1290</spage><epage>1296</epage><pages>1290-1296</pages><issn>1522-7235</issn><eissn>1522-7243</eissn><abstract>A new asymmetrical diarylethene containing a 1H‐imidazo [4,5‐f][1,10] phenanthroline unit was synthesized. The compound showed typical photochromism and functioned as a notable fluorescence switch upon alternating irradiation with ultraviolet (UV) and visible light. Its closed‐ring isomer could be used as a selective ‘naked‐eye’ colorimetric sensor for Cu2+, accompanied by a notable color change from blue to colorless. Furthermore, the compound was found to be selective towards Ca2+, Mg2+, and Sr2+ with significant fluorescence changes. On the basis of this characteristic, a logic circuit was constructed by utilizing both light and chemical stimuli as inputs and fluorescence intensity at 487 nm as output. Copyright © 2015 John Wiley &amp; Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25847126</pmid><doi>10.1002/bio.2895</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1522-7235
ispartof Luminescence (Chichester, England), 2015-12, Vol.30 (8), p.1290-1296
issn 1522-7235
1522-7243
language eng
recordid cdi_proquest_miscellaneous_1800483460
source Wiley-Blackwell Read & Publish Collection
subjects Asymmetry
cation recognition
Color
diarylethene
Ethylenes - chemistry
Fluorescence
Fluorescent Dyes - chemical synthesis
Fluorescent Dyes - chemistry
imidazole-containing substituent
Isomers
logic circuit
Luminescence
Luminous intensity
Molecular Structure
Phenanthrolines - chemistry
photochromism
Spectrometry, Fluorescence
Stimuli
Switches
title Multi-functional ion-sensor based on a photochromic diarylethene with a 1H-imidazo [4,5-f][1,10] phenanthroline unit
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T05%3A58%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Multi-functional%20ion-sensor%20based%20on%20a%20photochromic%20diarylethene%20with%20a%201H-imidazo%20%5B4,5-f%5D%5B1,10%5D%20phenanthroline%20unit&rft.jtitle=Luminescence%20(Chichester,%20England)&rft.au=Wang,%20Renjie&rft.date=2015-12&rft.volume=30&rft.issue=8&rft.spage=1290&rft.epage=1296&rft.pages=1290-1296&rft.issn=1522-7235&rft.eissn=1522-7243&rft_id=info:doi/10.1002/bio.2895&rft_dat=%3Cproquest_pubme%3E1800483460%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-i4185-df46a3fbe0dee1728096c27ccd368be56278db346417c46e3627c22b28d79ae03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1757116556&rft_id=info:pmid/25847126&rfr_iscdi=true