Surface modification strategy for fluorescence solvatochromism of carbon dots prepared from -phenylenediamine
The fluorescence solvatochromism of p -phenylenediamine-derived carbon dots (CDs) was modulated through surface modification with decanoic acid or perfluorodecanoic acid. This is attributed to the adjustment of the dipole interaction between solvent molecules and the CD surface in terms of steric hi...
Gespeichert in:
Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2020-02, Vol.56 (14), p.2174-2177 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2177 |
---|---|
container_issue | 14 |
container_start_page | 2174 |
container_title | Chemical communications (Cambridge, England) |
container_volume | 56 |
creator | Sato, Kohei Sato, Rina Iso, Yoshiki Isobe, Tetsuhiko |
description | The fluorescence solvatochromism of
p
-phenylenediamine-derived carbon dots (CDs) was modulated through surface modification with decanoic acid or perfluorodecanoic acid. This is attributed to the adjustment of the dipole interaction between solvent molecules and the CD surface in terms of steric hindrance of a surface modifier and polarization of the modified CD surface.
Surface modification of
p
-phenylenediamine-derived carbon dots with decanoic acid and perfluorodecanoic acid successfully modulated fluorescence solvatochromism. |
doi_str_mv | 10.1039/c9cc09333h |
format | Article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c9cc09333h</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c9cc09333h</sourcerecordid><originalsourceid>FETCH-rsc_primary_c9cc09333h3</originalsourceid><addsrcrecordid>eNqFj8FKxEAQRAdxwdX14l3oH4gmTKKbsyje9eBtaTs9ZiQzHbpnhfy9EQSP1qUKXtWhnLtq6pum9v0t9UR1770fT9y28Xdt1bX7t9Of3PXVvW-7M3du9lmvarr91qWXowYkhiRDDJGwRMlgRbHwxwJBFMJ0FGUjzmvNZPrCIjSqpGgJJAChvq-bQYrBrDyj8gBh5VDNI-dl4sxDxBQz79wm4GR8-esX7vrp8fXhuVKjw6wxoS6Hvw_-P_4Nq8NNXw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Surface modification strategy for fluorescence solvatochromism of carbon dots prepared from -phenylenediamine</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Sato, Kohei ; Sato, Rina ; Iso, Yoshiki ; Isobe, Tetsuhiko</creator><creatorcontrib>Sato, Kohei ; Sato, Rina ; Iso, Yoshiki ; Isobe, Tetsuhiko</creatorcontrib><description>The fluorescence solvatochromism of
p
-phenylenediamine-derived carbon dots (CDs) was modulated through surface modification with decanoic acid or perfluorodecanoic acid. This is attributed to the adjustment of the dipole interaction between solvent molecules and the CD surface in terms of steric hindrance of a surface modifier and polarization of the modified CD surface.
Surface modification of
p
-phenylenediamine-derived carbon dots with decanoic acid and perfluorodecanoic acid successfully modulated fluorescence solvatochromism.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c9cc09333h</identifier><ispartof>Chemical communications (Cambridge, England), 2020-02, Vol.56 (14), p.2174-2177</ispartof><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>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Sato, Kohei</creatorcontrib><creatorcontrib>Sato, Rina</creatorcontrib><creatorcontrib>Iso, Yoshiki</creatorcontrib><creatorcontrib>Isobe, Tetsuhiko</creatorcontrib><title>Surface modification strategy for fluorescence solvatochromism of carbon dots prepared from -phenylenediamine</title><title>Chemical communications (Cambridge, England)</title><description>The fluorescence solvatochromism of
p
-phenylenediamine-derived carbon dots (CDs) was modulated through surface modification with decanoic acid or perfluorodecanoic acid. This is attributed to the adjustment of the dipole interaction between solvent molecules and the CD surface in terms of steric hindrance of a surface modifier and polarization of the modified CD surface.
Surface modification of
p
-phenylenediamine-derived carbon dots with decanoic acid and perfluorodecanoic acid successfully modulated fluorescence solvatochromism.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj8FKxEAQRAdxwdX14l3oH4gmTKKbsyje9eBtaTs9ZiQzHbpnhfy9EQSP1qUKXtWhnLtq6pum9v0t9UR1770fT9y28Xdt1bX7t9Of3PXVvW-7M3du9lmvarr91qWXowYkhiRDDJGwRMlgRbHwxwJBFMJ0FGUjzmvNZPrCIjSqpGgJJAChvq-bQYrBrDyj8gBh5VDNI-dl4sxDxBQz79wm4GR8-esX7vrp8fXhuVKjw6wxoS6Hvw_-P_4Nq8NNXw</recordid><startdate>20200218</startdate><enddate>20200218</enddate><creator>Sato, Kohei</creator><creator>Sato, Rina</creator><creator>Iso, Yoshiki</creator><creator>Isobe, Tetsuhiko</creator><scope/></search><sort><creationdate>20200218</creationdate><title>Surface modification strategy for fluorescence solvatochromism of carbon dots prepared from -phenylenediamine</title><author>Sato, Kohei ; Sato, Rina ; Iso, Yoshiki ; Isobe, Tetsuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c9cc09333h3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Kohei</creatorcontrib><creatorcontrib>Sato, Rina</creatorcontrib><creatorcontrib>Iso, Yoshiki</creatorcontrib><creatorcontrib>Isobe, Tetsuhiko</creatorcontrib><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Kohei</au><au>Sato, Rina</au><au>Iso, Yoshiki</au><au>Isobe, Tetsuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface modification strategy for fluorescence solvatochromism of carbon dots prepared from -phenylenediamine</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><date>2020-02-18</date><risdate>2020</risdate><volume>56</volume><issue>14</issue><spage>2174</spage><epage>2177</epage><pages>2174-2177</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>The fluorescence solvatochromism of
p
-phenylenediamine-derived carbon dots (CDs) was modulated through surface modification with decanoic acid or perfluorodecanoic acid. This is attributed to the adjustment of the dipole interaction between solvent molecules and the CD surface in terms of steric hindrance of a surface modifier and polarization of the modified CD surface.
Surface modification of
p
-phenylenediamine-derived carbon dots with decanoic acid and perfluorodecanoic acid successfully modulated fluorescence solvatochromism.</abstract><doi>10.1039/c9cc09333h</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1359-7345 |
ispartof | Chemical communications (Cambridge, England), 2020-02, Vol.56 (14), p.2174-2177 |
issn | 1359-7345 1364-548X |
language | |
recordid | cdi_rsc_primary_c9cc09333h |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Surface modification strategy for fluorescence solvatochromism of carbon dots prepared from -phenylenediamine |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T14%3A19%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Surface%20modification%20strategy%20for%20fluorescence%20solvatochromism%20of%20carbon%20dots%20prepared%20from%20-phenylenediamine&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Sato,%20Kohei&rft.date=2020-02-18&rft.volume=56&rft.issue=14&rft.spage=2174&rft.epage=2177&rft.pages=2174-2177&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c9cc09333h&rft_dat=%3Crsc%3Ec9cc09333h%3C/rsc%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |