Efficient Catalysis of Phosphate Ester Hydrolysis by Bare Silica
This work reports the catalysis of bare silica materials (MCM-41, SBA-15, and silica gel) for the complete hydrolyses of bis(2,4-nitrophenyl)phosphate (BDNPP) and bis(4-nitrophenyl)phosphate (BNPP), which share the same phosphate diester chemical core with important biological molecules, DNA and R...
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container_title | Journal of physical chemistry. C |
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creator | Bahia, Samara B. B. B Amaya Vargas, Carlos A Denadai, Ângelo M. L Araujo, Maria Helena Moraes, Adolfo H Brandão, Tiago A. S |
description | This work reports the catalysis of bare silica materials (MCM-41, SBA-15, and silica gel) for the complete hydrolyses of bis(2,4-nitrophenyl)phosphate (BDNPP) and bis(4-nitrophenyl)phosphate (BNPP), which share the same phosphate diester chemical core with important biological molecules, DNA and RNA, and toxic substances like EA2192 and anatoxin-a(s). Catalytic effects above 7000-fold were observed for the hydrolysis of BNPP, which were consistent with a concerted SN2(P) mechanism under the action of siloxide and silanol groups that provide water activation by general base catalysis and leaving-group departure stabilization by general acid catalysis, respectively. We also observed that product formation follows a sigmoidal behavior as a result of catalytic effect enhancement following an induction period. This effect is discussed considering cooperative effects caused by silica hydration, which is unchanged upon material reuse affording strong catalytic effects for phosphate diester hydrolyses and no induction periods. |
doi_str_mv | 10.1021/acs.jpcc.0c04854 |
format | Article |
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We also observed that product formation follows a sigmoidal behavior as a result of catalytic effect enhancement following an induction period. This effect is discussed considering cooperative effects caused by silica hydration, which is unchanged upon material reuse affording strong catalytic effects for phosphate diester hydrolyses and no induction periods.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.0c04854</identifier><language>eng</language><publisher>WASHINGTON: American Chemical Society</publisher><subject>C: Surfaces, Interfaces, Porous Materials, and Catalysis ; Chemistry ; Chemistry, Physical ; Materials Science ; Materials Science, Multidisciplinary ; Nanoscience & Nanotechnology ; Physical Sciences ; Science & Technology ; Science & Technology - Other Topics ; Technology</subject><ispartof>Journal of physical chemistry. 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Catalytic effects above 7000-fold were observed for the hydrolysis of BNPP, which were consistent with a concerted SN2(P) mechanism under the action of siloxide and silanol groups that provide water activation by general base catalysis and leaving-group departure stabilization by general acid catalysis, respectively. We also observed that product formation follows a sigmoidal behavior as a result of catalytic effect enhancement following an induction period. This effect is discussed considering cooperative effects caused by silica hydration, which is unchanged upon material reuse affording strong catalytic effects for phosphate diester hydrolyses and no induction periods.</description><subject>C: Surfaces, Interfaces, Porous Materials, and Catalysis</subject><subject>Chemistry</subject><subject>Chemistry, Physical</subject><subject>Materials Science</subject><subject>Materials Science, Multidisciplinary</subject><subject>Nanoscience & Nanotechnology</subject><subject>Physical Sciences</subject><subject>Science & Technology</subject><subject>Science & Technology - Other Topics</subject><subject>Technology</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><recordid>eNqNkEtLAzEQgIMoWKt3j7nr1rz2dVOXaoWCgnpeJtmEptRNSVJk_72pW3oTPAwzMPMNMx9C15TMKGH0DlSYrbdKzYgiosrFCZrQmrOsFHl-eqxFeY4uQlgTknNC-QTdz42xyuo-4gYibIZgA3YGv61c2K4gajwPUXu8GDrvxq4c8CN4jd_txiq4RGcGNkFfHfIUfT7NP5pFtnx9fmkelhmwisSso0R0dSfzmlWcCJ5XwihVawq5BsZ0JwCEpkWpAVShJJSqq6k0TBpZUVLwKSLjXuVdCF6bduvtF_ihpaTdG2iTgXZvoD0YSEg1It9aOhP2Xyp9xEhyULAUNFW8bmyEaF3fuF0fE3rzfzRN347Tvye4ne-Tib_v-gEsGYDN</recordid><startdate>20200806</startdate><enddate>20200806</enddate><creator>Bahia, Samara B. 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L</creatorcontrib><creatorcontrib>Araujo, Maria Helena</creatorcontrib><creatorcontrib>Moraes, Adolfo H</creatorcontrib><creatorcontrib>Brandão, Tiago A. S</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>CrossRef</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bahia, Samara B. B. B</au><au>Amaya Vargas, Carlos A</au><au>Denadai, Ângelo M. L</au><au>Araujo, Maria Helena</au><au>Moraes, Adolfo H</au><au>Brandão, Tiago A. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Catalysis of Phosphate Ester Hydrolysis by Bare Silica</atitle><jtitle>Journal of physical chemistry. C</jtitle><stitle>J PHYS CHEM C</stitle><addtitle>J. Phys. Chem. C</addtitle><date>2020-08-06</date><risdate>2020</risdate><volume>124</volume><issue>31</issue><spage>17111</spage><epage>17120</epage><pages>17111-17120</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>This work reports the catalysis of bare silica materials (MCM-41, SBA-15, and silica gel) for the complete hydrolyses of bis(2,4-nitrophenyl)phosphate (BDNPP) and bis(4-nitrophenyl)phosphate (BNPP), which share the same phosphate diester chemical core with important biological molecules, DNA and RNA, and toxic substances like EA2192 and anatoxin-a(s). Catalytic effects above 7000-fold were observed for the hydrolysis of BNPP, which were consistent with a concerted SN2(P) mechanism under the action of siloxide and silanol groups that provide water activation by general base catalysis and leaving-group departure stabilization by general acid catalysis, respectively. 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subjects | C: Surfaces, Interfaces, Porous Materials, and Catalysis Chemistry Chemistry, Physical Materials Science Materials Science, Multidisciplinary Nanoscience & Nanotechnology Physical Sciences Science & Technology Science & Technology - Other Topics Technology |
title | Efficient Catalysis of Phosphate Ester Hydrolysis by Bare Silica |
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