Hydrazine functionalized probes for chromogenic and fluorescent ratiometric sensing of pH and F: experimental and DFT studies
Two novel hydrazine based sensors, BPPIH ( N 1 , N 3 -bis(perfluorophenyl)isophthalohydrazide) and BPBIH ( N 1′ , N 3′ -bis(perfluorobenzylidene)isophthalohydrazide), are presented here. BPPIH is found to be a highly sensitive pH sensor in the pH range 5.0 to 10.0 in a DMSO-water solvent mixture wit...
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creator | Roy Chowdhury, Additi Mondal, Amita Roy, Biswajit Gopal K, Jagadeesh C. Bose Mukhopadhyay, Sudit Banerjee, Priyabrata |
description | Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here.
BPPIH
is found to be a highly sensitive pH sensor in the pH range 5.0 to 10.0 in a DMSO-water solvent mixture with a p
K
a
value of 9.22. Interesting optical responses have been observed for
BPPIH
in the above mentioned pH range.
BPBIH
on the other hand turns out to be a less effective pH sensor in the above mentioned pH range. The increase in fluorescence intensity at a lower pH for
BPPIH
was explained by using density functional theory. The ability of
BPPIH
to monitor the pH changes inside cancer cells is a useful application of the sensor as a functional material. In addition fluoride (F
−
) selectivity studies of these two chemosensors have been performed and show that between them,
BPBIH
shows greater selectivity towards F
. The interaction energy calculated from the DFT-D3 supports the experimental findings. The pH sensor (
BPPIH
) can be further interfaced with suitable circuitry interfaced with desired programming for ease of access and enhancement of practical applications.
Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here. |
doi_str_mv | 10.1039/c7pp00246g |
format | Article |
fullrecord | <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_rsc_primary_c7pp00246g</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2010877662</sourcerecordid><originalsourceid>FETCH-LOGICAL-c451t-ae6daf3ef095be69473ba1545c4d0e3bd0cb34a626769388525a02ce6f620aed3</originalsourceid><addsrcrecordid>eNptkc9LHDEcxUNRXGu99K4EehHLtplMfsz0Jup2BaGXLfQ2ZJJv1pGZZExmQAX_98Zd3RXxlJD3yfvm5SH0NSM_MpKXP7Xse0IoE8tPaD9jkk1LUtKdzZ7_m6DPMd4SknEm5B6a0KLkghdyHz3NH0xQj40DbEenh8Y71TaPYHAffA0RWx-wvgm-80twjcbKGWzb0QeIGtyAg0p3OhhC0iK42Lgl9hb38xU5-4XhvofQdIlV7ersYrbAcRhNA_EL2rWqjXD4sh6gv7PLxfl8ev3n99X52fVUM54NUwXCKJuDJSWvQZRM5rVKWbhmhkBeG6LrnClBhRRlXhScckWoBmEFJQpMfoBO1r4p1N0Icai6Jj2_bZUDP8YqKxljuSScJvTbO_TWjyF9SqwoyUghpRDP1Oma0sHHGMBWfcqowkOVkeq5lGpbSoKPXyzHugOzQV9bSMD3NRCT5JYQtjM_tDta0yHqjdcb_T9NnaGj</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2010877662</pqid></control><display><type>article</type><title>Hydrazine functionalized probes for chromogenic and fluorescent ratiometric sensing of pH and F: experimental and DFT studies</title><source>SpringerLink Journals - AutoHoldings</source><creator>Roy Chowdhury, Additi ; Mondal, Amita ; Roy, Biswajit Gopal ; K, Jagadeesh C. Bose ; Mukhopadhyay, Sudit ; Banerjee, Priyabrata</creator><creatorcontrib>Roy Chowdhury, Additi ; Mondal, Amita ; Roy, Biswajit Gopal ; K, Jagadeesh C. Bose ; Mukhopadhyay, Sudit ; Banerjee, Priyabrata</creatorcontrib><description>Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here.
BPPIH
is found to be a highly sensitive pH sensor in the pH range 5.0 to 10.0 in a DMSO-water solvent mixture with a p
K
a
value of 9.22. Interesting optical responses have been observed for
BPPIH
in the above mentioned pH range.
BPBIH
on the other hand turns out to be a less effective pH sensor in the above mentioned pH range. The increase in fluorescence intensity at a lower pH for
BPPIH
was explained by using density functional theory. The ability of
BPPIH
to monitor the pH changes inside cancer cells is a useful application of the sensor as a functional material. In addition fluoride (F
−
) selectivity studies of these two chemosensors have been performed and show that between them,
BPBIH
shows greater selectivity towards F
. The interaction energy calculated from the DFT-D3 supports the experimental findings. The pH sensor (
BPPIH
) can be further interfaced with suitable circuitry interfaced with desired programming for ease of access and enhancement of practical applications.
Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here.</description><identifier>ISSN: 1474-905X</identifier><identifier>EISSN: 1474-9092</identifier><identifier>DOI: 10.1039/c7pp00246g</identifier><identifier>PMID: 28956587</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Biochemistry ; Biomaterials ; Cancer ; Chemical sensors ; Chemistry ; Chemoreceptors ; Circuits ; Density functional theory ; Fluorescence ; Fluorescent indicators ; Fluorides ; Hydrazine ; Hydrogen ions ; pH effects ; pH sensors ; Physical Chemistry ; Plant Sciences ; Selectivity ; Sensors</subject><ispartof>Photochemical & photobiological sciences, 2017, Vol.16 (11), p.1654-1663</ispartof><rights>The Royal Society of Chemistry and Owner Societies 2017</rights><rights>Copyright Royal Society of Chemistry 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-ae6daf3ef095be69473ba1545c4d0e3bd0cb34a626769388525a02ce6f620aed3</citedby><cites>FETCH-LOGICAL-c451t-ae6daf3ef095be69473ba1545c4d0e3bd0cb34a626769388525a02ce6f620aed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1039/c7pp00246g$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1039/c7pp00246g$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28956587$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roy Chowdhury, Additi</creatorcontrib><creatorcontrib>Mondal, Amita</creatorcontrib><creatorcontrib>Roy, Biswajit Gopal</creatorcontrib><creatorcontrib>K, Jagadeesh C. Bose</creatorcontrib><creatorcontrib>Mukhopadhyay, Sudit</creatorcontrib><creatorcontrib>Banerjee, Priyabrata</creatorcontrib><title>Hydrazine functionalized probes for chromogenic and fluorescent ratiometric sensing of pH and F: experimental and DFT studies</title><title>Photochemical & photobiological sciences</title><addtitle>Photochem Photobiol Sci</addtitle><addtitle>Photochem Photobiol Sci</addtitle><description>Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here.
BPPIH
is found to be a highly sensitive pH sensor in the pH range 5.0 to 10.0 in a DMSO-water solvent mixture with a p
K
a
value of 9.22. Interesting optical responses have been observed for
BPPIH
in the above mentioned pH range.
BPBIH
on the other hand turns out to be a less effective pH sensor in the above mentioned pH range. The increase in fluorescence intensity at a lower pH for
BPPIH
was explained by using density functional theory. The ability of
BPPIH
to monitor the pH changes inside cancer cells is a useful application of the sensor as a functional material. In addition fluoride (F
−
) selectivity studies of these two chemosensors have been performed and show that between them,
BPBIH
shows greater selectivity towards F
. The interaction energy calculated from the DFT-D3 supports the experimental findings. The pH sensor (
BPPIH
) can be further interfaced with suitable circuitry interfaced with desired programming for ease of access and enhancement of practical applications.
Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here.</description><subject>Biochemistry</subject><subject>Biomaterials</subject><subject>Cancer</subject><subject>Chemical sensors</subject><subject>Chemistry</subject><subject>Chemoreceptors</subject><subject>Circuits</subject><subject>Density functional theory</subject><subject>Fluorescence</subject><subject>Fluorescent indicators</subject><subject>Fluorides</subject><subject>Hydrazine</subject><subject>Hydrogen ions</subject><subject>pH effects</subject><subject>pH sensors</subject><subject>Physical Chemistry</subject><subject>Plant Sciences</subject><subject>Selectivity</subject><subject>Sensors</subject><issn>1474-905X</issn><issn>1474-9092</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNptkc9LHDEcxUNRXGu99K4EehHLtplMfsz0Jup2BaGXLfQ2ZJJv1pGZZExmQAX_98Zd3RXxlJD3yfvm5SH0NSM_MpKXP7Xse0IoE8tPaD9jkk1LUtKdzZ7_m6DPMd4SknEm5B6a0KLkghdyHz3NH0xQj40DbEenh8Y71TaPYHAffA0RWx-wvgm-80twjcbKGWzb0QeIGtyAg0p3OhhC0iK42Lgl9hb38xU5-4XhvofQdIlV7ersYrbAcRhNA_EL2rWqjXD4sh6gv7PLxfl8ev3n99X52fVUM54NUwXCKJuDJSWvQZRM5rVKWbhmhkBeG6LrnClBhRRlXhScckWoBmEFJQpMfoBO1r4p1N0Icai6Jj2_bZUDP8YqKxljuSScJvTbO_TWjyF9SqwoyUghpRDP1Oma0sHHGMBWfcqowkOVkeq5lGpbSoKPXyzHugOzQV9bSMD3NRCT5JYQtjM_tDta0yHqjdcb_T9NnaGj</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Roy Chowdhury, Additi</creator><creator>Mondal, Amita</creator><creator>Roy, Biswajit Gopal</creator><creator>K, Jagadeesh C. Bose</creator><creator>Mukhopadhyay, Sudit</creator><creator>Banerjee, Priyabrata</creator><general>Springer International Publishing</general><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2017</creationdate><title>Hydrazine functionalized probes for chromogenic and fluorescent ratiometric sensing of pH and F: experimental and DFT studies</title><author>Roy Chowdhury, Additi ; Mondal, Amita ; Roy, Biswajit Gopal ; K, Jagadeesh C. Bose ; Mukhopadhyay, Sudit ; Banerjee, Priyabrata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-ae6daf3ef095be69473ba1545c4d0e3bd0cb34a626769388525a02ce6f620aed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Biochemistry</topic><topic>Biomaterials</topic><topic>Cancer</topic><topic>Chemical sensors</topic><topic>Chemistry</topic><topic>Chemoreceptors</topic><topic>Circuits</topic><topic>Density functional theory</topic><topic>Fluorescence</topic><topic>Fluorescent indicators</topic><topic>Fluorides</topic><topic>Hydrazine</topic><topic>Hydrogen ions</topic><topic>pH effects</topic><topic>pH sensors</topic><topic>Physical Chemistry</topic><topic>Plant Sciences</topic><topic>Selectivity</topic><topic>Sensors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roy Chowdhury, Additi</creatorcontrib><creatorcontrib>Mondal, Amita</creatorcontrib><creatorcontrib>Roy, Biswajit Gopal</creatorcontrib><creatorcontrib>K, Jagadeesh C. Bose</creatorcontrib><creatorcontrib>Mukhopadhyay, Sudit</creatorcontrib><creatorcontrib>Banerjee, Priyabrata</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Photochemical & photobiological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roy Chowdhury, Additi</au><au>Mondal, Amita</au><au>Roy, Biswajit Gopal</au><au>K, Jagadeesh C. Bose</au><au>Mukhopadhyay, Sudit</au><au>Banerjee, Priyabrata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrazine functionalized probes for chromogenic and fluorescent ratiometric sensing of pH and F: experimental and DFT studies</atitle><jtitle>Photochemical & photobiological sciences</jtitle><stitle>Photochem Photobiol Sci</stitle><addtitle>Photochem Photobiol Sci</addtitle><date>2017</date><risdate>2017</risdate><volume>16</volume><issue>11</issue><spage>1654</spage><epage>1663</epage><pages>1654-1663</pages><issn>1474-905X</issn><eissn>1474-9092</eissn><abstract>Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here.
BPPIH
is found to be a highly sensitive pH sensor in the pH range 5.0 to 10.0 in a DMSO-water solvent mixture with a p
K
a
value of 9.22. Interesting optical responses have been observed for
BPPIH
in the above mentioned pH range.
BPBIH
on the other hand turns out to be a less effective pH sensor in the above mentioned pH range. The increase in fluorescence intensity at a lower pH for
BPPIH
was explained by using density functional theory. The ability of
BPPIH
to monitor the pH changes inside cancer cells is a useful application of the sensor as a functional material. In addition fluoride (F
−
) selectivity studies of these two chemosensors have been performed and show that between them,
BPBIH
shows greater selectivity towards F
. The interaction energy calculated from the DFT-D3 supports the experimental findings. The pH sensor (
BPPIH
) can be further interfaced with suitable circuitry interfaced with desired programming for ease of access and enhancement of practical applications.
Two novel hydrazine based sensors,
BPPIH
(
N
1
,
N
3
-bis(perfluorophenyl)isophthalohydrazide) and
BPBIH
(
N
1′
,
N
3′
-bis(perfluorobenzylidene)isophthalohydrazide), are presented here.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>28956587</pmid><doi>10.1039/c7pp00246g</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
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ispartof | Photochemical & photobiological sciences, 2017, Vol.16 (11), p.1654-1663 |
issn | 1474-905X 1474-9092 |
language | eng |
recordid | cdi_rsc_primary_c7pp00246g |
source | SpringerLink Journals - AutoHoldings |
subjects | Biochemistry Biomaterials Cancer Chemical sensors Chemistry Chemoreceptors Circuits Density functional theory Fluorescence Fluorescent indicators Fluorides Hydrazine Hydrogen ions pH effects pH sensors Physical Chemistry Plant Sciences Selectivity Sensors |
title | Hydrazine functionalized probes for chromogenic and fluorescent ratiometric sensing of pH and F: experimental and DFT studies |
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