author_facet Wang, De‐Gao
Li, Qian
Zhu, Yunlong
Tang, Hui
Song, Min
Kuang, Gui‐Chao
Wang, De‐Gao
Li, Qian
Zhu, Yunlong
Tang, Hui
Song, Min
Kuang, Gui‐Chao
author Wang, De‐Gao
Li, Qian
Zhu, Yunlong
Tang, Hui
Song, Min
Kuang, Gui‐Chao
spellingShingle Wang, De‐Gao
Li, Qian
Zhu, Yunlong
Tang, Hui
Song, Min
Kuang, Gui‐Chao
Macromolecular Chemistry and Physics
BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
Materials Chemistry
Organic Chemistry
Polymers and Plastics
Physical and Theoretical Chemistry
Condensed Matter Physics
author_sort wang, de‐gao
spelling Wang, De‐Gao Li, Qian Zhu, Yunlong Tang, Hui Song, Min Kuang, Gui‐Chao 1022-1352 1521-3935 Wiley Materials Chemistry Organic Chemistry Polymers and Plastics Physical and Theoretical Chemistry Condensed Matter Physics http://dx.doi.org/10.1002/macp.201700101 <jats:p>Facile Friedel–Crafts coupling reaction prepared porous organic polymers <jats:bold>BDP‐POP‐<jats:italic>n</jats:italic></jats:bold> (<jats:italic>n</jats:italic> = 1, 3, and 4) are reported. The influences of methyl substituents and single monomer isomerization on corresponding BDP‐POPs' porosity and singlet oxygen generation properties have been investigated. The obtained BDP‐POPs are thoroughly characterized by a combination of techniques such as Fourier transform infrared, solid <jats:sup>13</jats:sup>C NMR, scanning electron microscopy, and transmission electron microscopy. In addition, these porous polymers' singlet oxygen generation capacities under visible green light (480–510 nm) irradiation are compared. Results show that <jats:bold>BDP‐POP‐1</jats:bold>, whose pyrrolyl ring bears methyl substituents and the two 4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene (BDP) units are at <jats:italic>para</jats:italic>‐position of the phenyl ring, possesses the largest Brunauer–Emmett–Teller surface area and the best singlet oxygen generation ability. Control experiment reveals that the <jats:bold>BDP‐POP‐1</jats:bold> shows superiority in generating singlet oxygen than that of model polymer <jats:bold>CMPBDP</jats:bold>. It is believed that this work may pave a road to design more effective porous materials for photocatalysis. <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/macp201700101-abs-0001-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text></jats:p> BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation Macromolecular Chemistry and Physics
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title BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_unstemmed BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_full BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_fullStr BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_full_unstemmed BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_short BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_sort bodipy‐based porous organic polymers: how the monomeric methyl substituents and isomerization affect the porosity and singlet oxygen generation
topic Materials Chemistry
Organic Chemistry
Polymers and Plastics
Physical and Theoretical Chemistry
Condensed Matter Physics
url http://dx.doi.org/10.1002/macp.201700101
publishDate 2017
physical
description <jats:p>Facile Friedel–Crafts coupling reaction prepared porous organic polymers <jats:bold>BDP‐POP‐<jats:italic>n</jats:italic></jats:bold> (<jats:italic>n</jats:italic> = 1, 3, and 4) are reported. The influences of methyl substituents and single monomer isomerization on corresponding BDP‐POPs' porosity and singlet oxygen generation properties have been investigated. The obtained BDP‐POPs are thoroughly characterized by a combination of techniques such as Fourier transform infrared, solid <jats:sup>13</jats:sup>C NMR, scanning electron microscopy, and transmission electron microscopy. In addition, these porous polymers' singlet oxygen generation capacities under visible green light (480–510 nm) irradiation are compared. Results show that <jats:bold>BDP‐POP‐1</jats:bold>, whose pyrrolyl ring bears methyl substituents and the two 4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene (BDP) units are at <jats:italic>para</jats:italic>‐position of the phenyl ring, possesses the largest Brunauer–Emmett–Teller surface area and the best singlet oxygen generation ability. Control experiment reveals that the <jats:bold>BDP‐POP‐1</jats:bold> shows superiority in generating singlet oxygen than that of model polymer <jats:bold>CMPBDP</jats:bold>. It is believed that this work may pave a road to design more effective porous materials for photocatalysis. <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/macp201700101-abs-0001-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text></jats:p>
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author Wang, De‐Gao, Li, Qian, Zhu, Yunlong, Tang, Hui, Song, Min, Kuang, Gui‐Chao
author_facet Wang, De‐Gao, Li, Qian, Zhu, Yunlong, Tang, Hui, Song, Min, Kuang, Gui‐Chao, Wang, De‐Gao, Li, Qian, Zhu, Yunlong, Tang, Hui, Song, Min, Kuang, Gui‐Chao
author_sort wang, de‐gao
container_issue 15
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container_title Macromolecular Chemistry and Physics
container_volume 218
description <jats:p>Facile Friedel–Crafts coupling reaction prepared porous organic polymers <jats:bold>BDP‐POP‐<jats:italic>n</jats:italic></jats:bold> (<jats:italic>n</jats:italic> = 1, 3, and 4) are reported. The influences of methyl substituents and single monomer isomerization on corresponding BDP‐POPs' porosity and singlet oxygen generation properties have been investigated. The obtained BDP‐POPs are thoroughly characterized by a combination of techniques such as Fourier transform infrared, solid <jats:sup>13</jats:sup>C NMR, scanning electron microscopy, and transmission electron microscopy. In addition, these porous polymers' singlet oxygen generation capacities under visible green light (480–510 nm) irradiation are compared. Results show that <jats:bold>BDP‐POP‐1</jats:bold>, whose pyrrolyl ring bears methyl substituents and the two 4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene (BDP) units are at <jats:italic>para</jats:italic>‐position of the phenyl ring, possesses the largest Brunauer–Emmett–Teller surface area and the best singlet oxygen generation ability. Control experiment reveals that the <jats:bold>BDP‐POP‐1</jats:bold> shows superiority in generating singlet oxygen than that of model polymer <jats:bold>CMPBDP</jats:bold>. It is believed that this work may pave a road to design more effective porous materials for photocatalysis. <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/macp201700101-abs-0001-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text></jats:p>
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spelling Wang, De‐Gao Li, Qian Zhu, Yunlong Tang, Hui Song, Min Kuang, Gui‐Chao 1022-1352 1521-3935 Wiley Materials Chemistry Organic Chemistry Polymers and Plastics Physical and Theoretical Chemistry Condensed Matter Physics http://dx.doi.org/10.1002/macp.201700101 <jats:p>Facile Friedel–Crafts coupling reaction prepared porous organic polymers <jats:bold>BDP‐POP‐<jats:italic>n</jats:italic></jats:bold> (<jats:italic>n</jats:italic> = 1, 3, and 4) are reported. The influences of methyl substituents and single monomer isomerization on corresponding BDP‐POPs' porosity and singlet oxygen generation properties have been investigated. The obtained BDP‐POPs are thoroughly characterized by a combination of techniques such as Fourier transform infrared, solid <jats:sup>13</jats:sup>C NMR, scanning electron microscopy, and transmission electron microscopy. In addition, these porous polymers' singlet oxygen generation capacities under visible green light (480–510 nm) irradiation are compared. Results show that <jats:bold>BDP‐POP‐1</jats:bold>, whose pyrrolyl ring bears methyl substituents and the two 4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene (BDP) units are at <jats:italic>para</jats:italic>‐position of the phenyl ring, possesses the largest Brunauer–Emmett–Teller surface area and the best singlet oxygen generation ability. Control experiment reveals that the <jats:bold>BDP‐POP‐1</jats:bold> shows superiority in generating singlet oxygen than that of model polymer <jats:bold>CMPBDP</jats:bold>. It is believed that this work may pave a road to design more effective porous materials for photocatalysis. <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/macp201700101-abs-0001-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text></jats:p> BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation Macromolecular Chemistry and Physics
spellingShingle Wang, De‐Gao, Li, Qian, Zhu, Yunlong, Tang, Hui, Song, Min, Kuang, Gui‐Chao, Macromolecular Chemistry and Physics, BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation, Materials Chemistry, Organic Chemistry, Polymers and Plastics, Physical and Theoretical Chemistry, Condensed Matter Physics
title BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_full BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_fullStr BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_full_unstemmed BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_short BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
title_sort bodipy‐based porous organic polymers: how the monomeric methyl substituents and isomerization affect the porosity and singlet oxygen generation
title_unstemmed BODIPY‐Based Porous Organic Polymers: How the Monomeric Methyl Substituents and Isomerization Affect the Porosity and Singlet Oxygen Generation
topic Materials Chemistry, Organic Chemistry, Polymers and Plastics, Physical and Theoretical Chemistry, Condensed Matter Physics
url http://dx.doi.org/10.1002/macp.201700101