AIEE phenomenon: tetraaryl vs. triaryl pyrazoles

Tetraarylpyrazoles are synthesized from commercially available materials in three steps and found to exhibit Aggregation Induced Emission Enhancement (AIEE) characteristics. Removing one aryl unit from tetraarylpyrazole leads to Aggregation Caused Quenching (ACQ), thus the number of aryl groups play...

Full description

Saved in:
Bibliographic Details
Published in:Chemical communications (Cambridge, England) England), 2015-01, Vol.51 (96), p.17148-17151
Main Authors: Mukherjee, Sayani, Salini, P S, Srinivasan, A, Peruncheralathan, S
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c287t-54554a3d4be3c344e0c117f2ec1df01dc023c416825cf2e57af7e8af7eb2bfa53
cites cdi_FETCH-LOGICAL-c287t-54554a3d4be3c344e0c117f2ec1df01dc023c416825cf2e57af7e8af7eb2bfa53
container_end_page 17151
container_issue 96
container_start_page 17148
container_title Chemical communications (Cambridge, England)
container_volume 51
creator Mukherjee, Sayani
Salini, P S
Srinivasan, A
Peruncheralathan, S
description Tetraarylpyrazoles are synthesized from commercially available materials in three steps and found to exhibit Aggregation Induced Emission Enhancement (AIEE) characteristics. Removing one aryl unit from tetraarylpyrazole leads to Aggregation Caused Quenching (ACQ), thus the number of aryl groups plays an important role in exploring such a phenomenon.
doi_str_mv 10.1039/c5cc05973a
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1735328743</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1735328743</sourcerecordid><originalsourceid>FETCH-LOGICAL-c287t-54554a3d4be3c344e0c117f2ec1df01dc023c416825cf2e57af7e8af7eb2bfa53</originalsourceid><addsrcrecordid>eNo9UE1Lw0AQXUSxtXrxB0iOIqTuZna6ibcQqhYKXhS8hc1mgpV8uZsI9de7_dCBmXkMjzePx9i14HPBIbk3aAzHRIE-YVMBCxmijN9PdxiTUIHECbtw7pP7Ehifs0m0kIgg5JTxdLVcBv0HtV3ju30IBhqs1nZbB99uHgx2s8f91uqfriZ3yc4qXTu6Ou4Ze3tcvmbP4frlaZWl69BEsRq8A0SpoZQFgQEpiRshVBWREWXFRWl4BEaKRRyh8VdUulIU70YRFZVGmLHbg25vu6-R3JA3G2eornVL3ehyoQDBv5LgqXcHqrGdc5aqvLebxtvOBc93CeUZZtk-odSTb466Y9FQ-U_9iwR-AR6DYDI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1735328743</pqid></control><display><type>article</type><title>AIEE phenomenon: tetraaryl vs. triaryl pyrazoles</title><source>Royal Society of Chemistry Journals</source><creator>Mukherjee, Sayani ; Salini, P S ; Srinivasan, A ; Peruncheralathan, S</creator><creatorcontrib>Mukherjee, Sayani ; Salini, P S ; Srinivasan, A ; Peruncheralathan, S</creatorcontrib><description>Tetraarylpyrazoles are synthesized from commercially available materials in three steps and found to exhibit Aggregation Induced Emission Enhancement (AIEE) characteristics. Removing one aryl unit from tetraarylpyrazole leads to Aggregation Caused Quenching (ACQ), thus the number of aryl groups plays an important role in exploring such a phenomenon.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c5cc05973a</identifier><identifier>PMID: 26455314</identifier><language>eng</language><publisher>England</publisher><ispartof>Chemical communications (Cambridge, England), 2015-01, Vol.51 (96), p.17148-17151</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c287t-54554a3d4be3c344e0c117f2ec1df01dc023c416825cf2e57af7e8af7eb2bfa53</citedby><cites>FETCH-LOGICAL-c287t-54554a3d4be3c344e0c117f2ec1df01dc023c416825cf2e57af7e8af7eb2bfa53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26455314$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukherjee, Sayani</creatorcontrib><creatorcontrib>Salini, P S</creatorcontrib><creatorcontrib>Srinivasan, A</creatorcontrib><creatorcontrib>Peruncheralathan, S</creatorcontrib><title>AIEE phenomenon: tetraaryl vs. triaryl pyrazoles</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>Tetraarylpyrazoles are synthesized from commercially available materials in three steps and found to exhibit Aggregation Induced Emission Enhancement (AIEE) characteristics. Removing one aryl unit from tetraarylpyrazole leads to Aggregation Caused Quenching (ACQ), thus the number of aryl groups plays an important role in exploring such a phenomenon.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNo9UE1Lw0AQXUSxtXrxB0iOIqTuZna6ibcQqhYKXhS8hc1mgpV8uZsI9de7_dCBmXkMjzePx9i14HPBIbk3aAzHRIE-YVMBCxmijN9PdxiTUIHECbtw7pP7Ehifs0m0kIgg5JTxdLVcBv0HtV3ju30IBhqs1nZbB99uHgx2s8f91uqfriZ3yc4qXTu6Ou4Ze3tcvmbP4frlaZWl69BEsRq8A0SpoZQFgQEpiRshVBWREWXFRWl4BEaKRRyh8VdUulIU70YRFZVGmLHbg25vu6-R3JA3G2eornVL3ehyoQDBv5LgqXcHqrGdc5aqvLebxtvOBc93CeUZZtk-odSTb466Y9FQ-U_9iwR-AR6DYDI</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Mukherjee, Sayani</creator><creator>Salini, P S</creator><creator>Srinivasan, A</creator><creator>Peruncheralathan, S</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150101</creationdate><title>AIEE phenomenon: tetraaryl vs. triaryl pyrazoles</title><author>Mukherjee, Sayani ; Salini, P S ; Srinivasan, A ; Peruncheralathan, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c287t-54554a3d4be3c344e0c117f2ec1df01dc023c416825cf2e57af7e8af7eb2bfa53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukherjee, Sayani</creatorcontrib><creatorcontrib>Salini, P S</creatorcontrib><creatorcontrib>Srinivasan, A</creatorcontrib><creatorcontrib>Peruncheralathan, S</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukherjee, Sayani</au><au>Salini, P S</au><au>Srinivasan, A</au><au>Peruncheralathan, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AIEE phenomenon: tetraaryl vs. triaryl pyrazoles</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>51</volume><issue>96</issue><spage>17148</spage><epage>17151</epage><pages>17148-17151</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Tetraarylpyrazoles are synthesized from commercially available materials in three steps and found to exhibit Aggregation Induced Emission Enhancement (AIEE) characteristics. Removing one aryl unit from tetraarylpyrazole leads to Aggregation Caused Quenching (ACQ), thus the number of aryl groups plays an important role in exploring such a phenomenon.</abstract><cop>England</cop><pmid>26455314</pmid><doi>10.1039/c5cc05973a</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1359-7345
ispartof Chemical communications (Cambridge, England), 2015-01, Vol.51 (96), p.17148-17151
issn 1359-7345
1364-548X
language eng
recordid cdi_proquest_miscellaneous_1735328743
source Royal Society of Chemistry Journals
title AIEE phenomenon: tetraaryl vs. triaryl pyrazoles
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T19%3A50%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=AIEE%20phenomenon:%20tetraaryl%20vs.%20triaryl%20pyrazoles&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Mukherjee,%20Sayani&rft.date=2015-01-01&rft.volume=51&rft.issue=96&rft.spage=17148&rft.epage=17151&rft.pages=17148-17151&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c5cc05973a&rft_dat=%3Cproquest_cross%3E1735328743%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c287t-54554a3d4be3c344e0c117f2ec1df01dc023c416825cf2e57af7e8af7eb2bfa53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1735328743&rft_id=info:pmid/26455314&rfr_iscdi=true