Fluorescent Cadmium Bipillared‐Layer Open Frameworks: Synthesis, Structures, Sensing of Nitro Compounds, and Capture of Volatile Iodine

Fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐...

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Veröffentlicht in:Chemistry : a European journal 2019-01, Vol.25 (5), p.1337-1344
Hauptverfasser: Chen, Tang‐Ching, Tsai, Meng‐Jung, Wu, Jing‐Yun
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description Fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐yl)‐4‐(pyridin‐4‐yl)‐1,8‐naphthalimide)), featuring non‐ and twofold interpenetrating pcu‐type bipillared‐layer open structures with sufficient free voids of 58.4, 51.4, 51.5, and 41.4 %, respectively, have been hydro(solvo)thermally synthesized. MOFs 1–4 emitted solid‐state blue or cyan fluorescence emissions at 447±7 nm, which mainly arose from NI‐bpy‐44 and are dependent on the incorporated solvents. After immersing the crystalline samples in different solvents, that is, H2O and DMSO (1 and 2) as well as nitrobenzene and phenol (1–4), they exhibited a remarkable fluorescence quenching effect, whereas o‐xylene and p‐xylene (4) caused significant fluorescence enhancement. The sensing ability of MOFs 1–4 toward nitro compounds carried out in the vapor phase showed that nitrobenzene and 2‐nitrophenol displayed detectable fluorescence quenching with 1, 2, and 4 whereas 4‐nitrotoluene was an effective fluorescence quencher for 1 and 2; this is most likely attributed to their electron‐deficient properties and higher vapor pressures. Moreover, MOFs 1–4 are highly reusable for quick capture of volatile iodine, as supported by clear crystal color change and also by immense fluorescence quenching responses owing to the donor–acceptor interaction. Low‐pressure CO2 adsorption isotherms indicate that activated materials 1′–4′ are inefficient at taking up CO2. Cube root: The synthesis and crystal structures of four fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐yl)‐4‐(pyridin‐4‐yl)‐1,8‐naphthalimide), featuring a pcu‐type bipillared‐layer open framework, and their potential for sensing small organic molecules and iodine capture are reported.
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MOFs 1–4 emitted solid‐state blue or cyan fluorescence emissions at 447±7 nm, which mainly arose from NI‐bpy‐44 and are dependent on the incorporated solvents. After immersing the crystalline samples in different solvents, that is, H2O and DMSO (1 and 2) as well as nitrobenzene and phenol (1–4), they exhibited a remarkable fluorescence quenching effect, whereas o‐xylene and p‐xylene (4) caused significant fluorescence enhancement. The sensing ability of MOFs 1–4 toward nitro compounds carried out in the vapor phase showed that nitrobenzene and 2‐nitrophenol displayed detectable fluorescence quenching with 1, 2, and 4 whereas 4‐nitrotoluene was an effective fluorescence quencher for 1 and 2; this is most likely attributed to their electron‐deficient properties and higher vapor pressures. Moreover, MOFs 1–4 are highly reusable for quick capture of volatile iodine, as supported by clear crystal color change and also by immense fluorescence quenching responses owing to the donor–acceptor interaction. Low‐pressure CO2 adsorption isotherms indicate that activated materials 1′–4′ are inefficient at taking up CO2. Cube root: The synthesis and crystal structures of four fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐yl)‐4‐(pyridin‐4‐yl)‐1,8‐naphthalimide), featuring a pcu‐type bipillared‐layer open framework, and their potential for sensing small organic molecules and iodine capture are reported.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.201804673</identifier><identifier>PMID: 30393906</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Benzene ; Biphenyl ; Bromobenzene ; Cadmium ; Carbon dioxide ; Chemistry ; Fluorescence ; Iodine ; Metal-organic frameworks ; Nitro compounds ; Nitrobenzene ; Nitrogen dioxide ; Nitrophenol ; Nitrotoluene ; Phenols ; Quenching ; Solvents ; Vapor phases ; Vapors ; Xylene</subject><ispartof>Chemistry : a European journal, 2019-01, Vol.25 (5), p.1337-1344</ispartof><rights>2019 Wiley‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2018 Wiley-VCH Verlag GmbH &amp; Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4103-704f0f8550dceff039caad14673dbc5bf319d0f2abc6a8f3f86c8f223981869c3</citedby><cites>FETCH-LOGICAL-c4103-704f0f8550dceff039caad14673dbc5bf319d0f2abc6a8f3f86c8f223981869c3</cites><orcidid>0000-0002-7257-4711</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchem.201804673$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchem.201804673$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30393906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Tang‐Ching</creatorcontrib><creatorcontrib>Tsai, Meng‐Jung</creatorcontrib><creatorcontrib>Wu, Jing‐Yun</creatorcontrib><title>Fluorescent Cadmium Bipillared‐Layer Open Frameworks: Synthesis, Structures, Sensing of Nitro Compounds, and Capture of Volatile Iodine</title><title>Chemistry : a European journal</title><addtitle>Chemistry</addtitle><description>Fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐yl)‐4‐(pyridin‐4‐yl)‐1,8‐naphthalimide)), featuring non‐ and twofold interpenetrating pcu‐type bipillared‐layer open structures with sufficient free voids of 58.4, 51.4, 51.5, and 41.4 %, respectively, have been hydro(solvo)thermally synthesized. MOFs 1–4 emitted solid‐state blue or cyan fluorescence emissions at 447±7 nm, which mainly arose from NI‐bpy‐44 and are dependent on the incorporated solvents. After immersing the crystalline samples in different solvents, that is, H2O and DMSO (1 and 2) as well as nitrobenzene and phenol (1–4), they exhibited a remarkable fluorescence quenching effect, whereas o‐xylene and p‐xylene (4) caused significant fluorescence enhancement. The sensing ability of MOFs 1–4 toward nitro compounds carried out in the vapor phase showed that nitrobenzene and 2‐nitrophenol displayed detectable fluorescence quenching with 1, 2, and 4 whereas 4‐nitrotoluene was an effective fluorescence quencher for 1 and 2; this is most likely attributed to their electron‐deficient properties and higher vapor pressures. Moreover, MOFs 1–4 are highly reusable for quick capture of volatile iodine, as supported by clear crystal color change and also by immense fluorescence quenching responses owing to the donor–acceptor interaction. Low‐pressure CO2 adsorption isotherms indicate that activated materials 1′–4′ are inefficient at taking up CO2. Cube root: The synthesis and crystal structures of four fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐yl)‐4‐(pyridin‐4‐yl)‐1,8‐naphthalimide), featuring a pcu‐type bipillared‐layer open framework, and their potential for sensing small organic molecules and iodine capture are reported.</description><subject>Benzene</subject><subject>Biphenyl</subject><subject>Bromobenzene</subject><subject>Cadmium</subject><subject>Carbon dioxide</subject><subject>Chemistry</subject><subject>Fluorescence</subject><subject>Iodine</subject><subject>Metal-organic frameworks</subject><subject>Nitro compounds</subject><subject>Nitrobenzene</subject><subject>Nitrogen dioxide</subject><subject>Nitrophenol</subject><subject>Nitrotoluene</subject><subject>Phenols</subject><subject>Quenching</subject><subject>Solvents</subject><subject>Vapor phases</subject><subject>Vapors</subject><subject>Xylene</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS0EosvClSOyxIUD2Y7jjRNzg6jbVtrSQ4Fr5PUf6pLYwY5V7Y0rNz4jn6SOthSJC6exND-_mTcPoZcEVgSgPJbXeliVQBpYs5o-QgtSlaSgNaseowXwdV2wivIj9CzGGwDgjNKn6IgC5ZQDW6Cfmz75oKPUbsKtUINNA_5gR9v3Imj1-8evrdjrgC9H7fAmiEHf-vAtvsNXezdd62jjW3w1hSSnlFXyW7to3VfsDf5op-Bx64fRJ6dyTziVR4wzOfe_-F5Mttf43Cvr9HP0xIg-6hf3dYk-b04-tWfF9vL0vH2_LeSaAC1qWBswTVWBktqYbEQKocjsXu1ktTOUcAWmFDvJRGOoaZhsTFlS3pCGcUmX6M1Bdwz-e9Jx6gab7We_TvsUu5JQgKpi-VJL9Pof9Man4PJ2maqhKSlrWKZWB0oGH2PQphuDHUTYdwS6OaRuDql7CCl_eHUvm3aDVg_4n1QywA_AbT7P_j9yXXt2cvFX_A5_CKBu</recordid><startdate>20190124</startdate><enddate>20190124</enddate><creator>Chen, Tang‐Ching</creator><creator>Tsai, Meng‐Jung</creator><creator>Wu, Jing‐Yun</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7257-4711</orcidid></search><sort><creationdate>20190124</creationdate><title>Fluorescent Cadmium Bipillared‐Layer Open Frameworks: Synthesis, Structures, Sensing of Nitro Compounds, and Capture of Volatile Iodine</title><author>Chen, Tang‐Ching ; Tsai, Meng‐Jung ; Wu, Jing‐Yun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4103-704f0f8550dceff039caad14673dbc5bf319d0f2abc6a8f3f86c8f223981869c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Benzene</topic><topic>Biphenyl</topic><topic>Bromobenzene</topic><topic>Cadmium</topic><topic>Carbon dioxide</topic><topic>Chemistry</topic><topic>Fluorescence</topic><topic>Iodine</topic><topic>Metal-organic frameworks</topic><topic>Nitro compounds</topic><topic>Nitrobenzene</topic><topic>Nitrogen dioxide</topic><topic>Nitrophenol</topic><topic>Nitrotoluene</topic><topic>Phenols</topic><topic>Quenching</topic><topic>Solvents</topic><topic>Vapor phases</topic><topic>Vapors</topic><topic>Xylene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Tang‐Ching</creatorcontrib><creatorcontrib>Tsai, Meng‐Jung</creatorcontrib><creatorcontrib>Wu, Jing‐Yun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Tang‐Ching</au><au>Tsai, Meng‐Jung</au><au>Wu, Jing‐Yun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorescent Cadmium Bipillared‐Layer Open Frameworks: Synthesis, Structures, Sensing of Nitro Compounds, and Capture of Volatile Iodine</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2019-01-24</date><risdate>2019</risdate><volume>25</volume><issue>5</issue><spage>1337</spage><epage>1344</epage><pages>1337-1344</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>Fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐yl)‐4‐(pyridin‐4‐yl)‐1,8‐naphthalimide)), featuring non‐ and twofold interpenetrating pcu‐type bipillared‐layer open structures with sufficient free voids of 58.4, 51.4, 51.5, and 41.4 %, respectively, have been hydro(solvo)thermally synthesized. MOFs 1–4 emitted solid‐state blue or cyan fluorescence emissions at 447±7 nm, which mainly arose from NI‐bpy‐44 and are dependent on the incorporated solvents. After immersing the crystalline samples in different solvents, that is, H2O and DMSO (1 and 2) as well as nitrobenzene and phenol (1–4), they exhibited a remarkable fluorescence quenching effect, whereas o‐xylene and p‐xylene (4) caused significant fluorescence enhancement. The sensing ability of MOFs 1–4 toward nitro compounds carried out in the vapor phase showed that nitrobenzene and 2‐nitrophenol displayed detectable fluorescence quenching with 1, 2, and 4 whereas 4‐nitrotoluene was an effective fluorescence quencher for 1 and 2; this is most likely attributed to their electron‐deficient properties and higher vapor pressures. Moreover, MOFs 1–4 are highly reusable for quick capture of volatile iodine, as supported by clear crystal color change and also by immense fluorescence quenching responses owing to the donor–acceptor interaction. Low‐pressure CO2 adsorption isotherms indicate that activated materials 1′–4′ are inefficient at taking up CO2. Cube root: The synthesis and crystal structures of four fluorescent Cd metal–organic frameworks (MOFs), [Cd2(dicarboxylate)2(NI‐bpy‐44)2] (dicarboxylate=benzene‐1,4‐dicarboxylate (1,4‐bdc, 1), 2‐bromobenzene‐1,4‐dicarboxylate (Br‐1,4‐bdc, 2), 2‐nitrobenzene‐1,4‐dicarboxylate (NO2‐1,4‐bdc, 3), biphenyl‐4,4′‐dicarboxylate (bpdc, 4); NI‐bpy‐44=N‐(pyridin‐4‐yl)‐4‐(pyridin‐4‐yl)‐1,8‐naphthalimide), featuring a pcu‐type bipillared‐layer open framework, and their potential for sensing small organic molecules and iodine capture are reported.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30393906</pmid><doi>10.1002/chem.201804673</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-7257-4711</orcidid></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Benzene
Biphenyl
Bromobenzene
Cadmium
Carbon dioxide
Chemistry
Fluorescence
Iodine
Metal-organic frameworks
Nitro compounds
Nitrobenzene
Nitrogen dioxide
Nitrophenol
Nitrotoluene
Phenols
Quenching
Solvents
Vapor phases
Vapors
Xylene
title Fluorescent Cadmium Bipillared‐Layer Open Frameworks: Synthesis, Structures, Sensing of Nitro Compounds, and Capture of Volatile Iodine
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