Cobalt Schiff-base complexes for electrocatalytic hydrogen generationElectronic supplementary information (ESI) available. CCDC 1549635 and 1549636. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7dt01750b
Two cobalt( iii ) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials. The dinitro and tetranitro derivatized Schiff-base complexes show catalytic activity at −0.96 V and −1.1 V vs. Fc + /Fc, respectively, resulting in overpote...
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creator | DiRisio, Ryan J Armstrong, Jessica E Frank, Mariah A Lake, William R McNamara, William R |
description | Two cobalt(
iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials. The dinitro and tetranitro derivatized Schiff-base complexes show catalytic activity at −0.96 V and −1.1 V
vs.
Fc
+
/Fc, respectively, resulting in overpotentials of 120 mV and 280 mV. Foot-of-the-wave analysis is used to examine the kinetic properties of these complexes, yielding a theoretical TOF
max
of up to 4100 s
−1
. Experimental TOFs of 7 s
−1
and 3 s
−1
are observed. Catalytic Tafel plots are also presented in order to benchmark the relationship between turnover frequency and overpotential.
Two cobalt(
iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials. |
doi_str_mv | 10.1039/c7dt01750b |
format | Article |
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iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials. The dinitro and tetranitro derivatized Schiff-base complexes show catalytic activity at −0.96 V and −1.1 V
vs.
Fc
+
/Fc, respectively, resulting in overpotentials of 120 mV and 280 mV. Foot-of-the-wave analysis is used to examine the kinetic properties of these complexes, yielding a theoretical TOF
max
of up to 4100 s
−1
. Experimental TOFs of 7 s
−1
and 3 s
−1
are observed. Catalytic Tafel plots are also presented in order to benchmark the relationship between turnover frequency and overpotential.
Two cobalt(
iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c7dt01750b</identifier><language>eng</language><creationdate>2017-08</creationdate><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>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>DiRisio, Ryan J</creatorcontrib><creatorcontrib>Armstrong, Jessica E</creatorcontrib><creatorcontrib>Frank, Mariah A</creatorcontrib><creatorcontrib>Lake, William R</creatorcontrib><creatorcontrib>McNamara, William R</creatorcontrib><title>Cobalt Schiff-base complexes for electrocatalytic hydrogen generationElectronic supplementary information (ESI) available. CCDC 1549635 and 1549636. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7dt01750b</title><description>Two cobalt(
iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials. The dinitro and tetranitro derivatized Schiff-base complexes show catalytic activity at −0.96 V and −1.1 V
vs.
Fc
+
/Fc, respectively, resulting in overpotentials of 120 mV and 280 mV. Foot-of-the-wave analysis is used to examine the kinetic properties of these complexes, yielding a theoretical TOF
max
of up to 4100 s
−1
. Experimental TOFs of 7 s
−1
and 3 s
−1
are observed. Catalytic Tafel plots are also presented in order to benchmark the relationship between turnover frequency and overpotential.
Two cobalt(
iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials.</description><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkLtOxDAQRS0EEsujoUcaOigSnLdC603EVhRLHznOZBPkxJFtEPlvPgDvQ0uBBIU1o7nHc6-GkJuA-gGN8keRNZYGWULrE7II4izz8jCKT499mJ6TC2PeKA1DmoQL8sVUzaWFtej6tvVqbhCEGiaJn2igVRpQorBaCW65nG0voJsbrTY4gnuoue3VWOyZ0anmfXKfBxwt1zP0o1sx7Bi4L9arB-AfvJe8lugDY0sGQRLnaZQAH5tDn_pQOl9H74ZCz8ZZS7XRfOqcQ-OSuMXAViU4TtkOjym3CfaOYBBh-bJ6gt-3uSJnLZcGrw_1ktyWxSt79rQR1aT7wUWvfvDof_3uL72amjb6Bp-Dgpc</recordid><startdate>20170808</startdate><enddate>20170808</enddate><creator>DiRisio, Ryan J</creator><creator>Armstrong, Jessica E</creator><creator>Frank, Mariah A</creator><creator>Lake, William R</creator><creator>McNamara, William R</creator><scope/></search><sort><creationdate>20170808</creationdate><title>Cobalt Schiff-base complexes for electrocatalytic hydrogen generationElectronic supplementary information (ESI) available. CCDC 1549635 and 1549636. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7dt01750b</title><author>DiRisio, Ryan J ; Armstrong, Jessica E ; Frank, Mariah A ; Lake, William R ; McNamara, William R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c7dt01750b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DiRisio, Ryan J</creatorcontrib><creatorcontrib>Armstrong, Jessica E</creatorcontrib><creatorcontrib>Frank, Mariah A</creatorcontrib><creatorcontrib>Lake, William R</creatorcontrib><creatorcontrib>McNamara, William R</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DiRisio, Ryan J</au><au>Armstrong, Jessica E</au><au>Frank, Mariah A</au><au>Lake, William R</au><au>McNamara, William R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cobalt Schiff-base complexes for electrocatalytic hydrogen generationElectronic supplementary information (ESI) available. CCDC 1549635 and 1549636. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7dt01750b</atitle><date>2017-08-08</date><risdate>2017</risdate><volume>46</volume><issue>31</issue><spage>1418</spage><epage>1425</epage><pages>1418-1425</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>Two cobalt(
iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials. The dinitro and tetranitro derivatized Schiff-base complexes show catalytic activity at −0.96 V and −1.1 V
vs.
Fc
+
/Fc, respectively, resulting in overpotentials of 120 mV and 280 mV. Foot-of-the-wave analysis is used to examine the kinetic properties of these complexes, yielding a theoretical TOF
max
of up to 4100 s
−1
. Experimental TOFs of 7 s
−1
and 3 s
−1
are observed. Catalytic Tafel plots are also presented in order to benchmark the relationship between turnover frequency and overpotential.
Two cobalt(
iii
) complexes containing inexpensive Schiff-base ligands have been found to be active for proton reduction at low overpotentials.</abstract><doi>10.1039/c7dt01750b</doi><tpages>8</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Cobalt Schiff-base complexes for electrocatalytic hydrogen generationElectronic supplementary information (ESI) available. CCDC 1549635 and 1549636. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7dt01750b |
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