Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents
Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescei...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Zhang, Shuo [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2021transfer abstract |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study - Fitzgerald, Emily ELSEVIER, 2020, the international journal for the science and technology of polymers, Oxford |
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| Übergeordnetes Werk: |
volume:226 ; year:2021 ; day:4 ; month:06 ; pages:0 |
| Links: |
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| DOI / URN: |
10.1016/j.polymer.2021.123840 |
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| 520 | |a Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). | ||
| 520 | |a Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). | ||
| 650 | 7 | |a BODIPY |2 Elsevier | |
| 650 | 7 | |a Carboxyfluorescein |2 Elsevier | |
| 650 | 7 | |a Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation |2 Elsevier | |
| 700 | 1 | |a Zhang, Yichuan |4 oth | |
| 700 | 1 | |a Üçüncü, Muhammed |4 oth | |
| 700 | 1 | |a Lilienkampf, Annamaria |4 oth | |
| 700 | 1 | |a Geng, Jin |4 oth | |
| 700 | 1 | |a Bradley, Mark |4 oth | |
| 773 | 0 | 8 | |i Enthalten in |n Elsevier Science |a Fitzgerald, Emily ELSEVIER |t Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study |d 2020 |d the international journal for the science and technology of polymers |g Oxford |w (DE-627)ELV005093368 |
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10.1016/j.polymer.2021.123840 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001613.pica (DE-627)ELV054121116 (ELSEVIER)S0032-3861(21)00463-8 DE-627 ger DE-627 rakwb eng 610 VZ 44.63 bkl 44.69 bkl Zhang, Shuo verfasserin aut Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents 2021transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). BODIPY Elsevier Carboxyfluorescein Elsevier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation Elsevier Zhang, Yichuan oth Üçüncü, Muhammed oth Lilienkampf, Annamaria oth Geng, Jin oth Bradley, Mark oth Enthalten in Elsevier Science Fitzgerald, Emily ELSEVIER Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study 2020 the international journal for the science and technology of polymers Oxford (DE-627)ELV005093368 volume:226 year:2021 day:4 month:06 pages:0 https://doi.org/10.1016/j.polymer.2021.123840 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.63 Krankenpflege VZ 44.69 Intensivmedizin VZ AR 226 2021 4 0604 0 |
| spelling |
10.1016/j.polymer.2021.123840 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001613.pica (DE-627)ELV054121116 (ELSEVIER)S0032-3861(21)00463-8 DE-627 ger DE-627 rakwb eng 610 VZ 44.63 bkl 44.69 bkl Zhang, Shuo verfasserin aut Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents 2021transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). BODIPY Elsevier Carboxyfluorescein Elsevier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation Elsevier Zhang, Yichuan oth Üçüncü, Muhammed oth Lilienkampf, Annamaria oth Geng, Jin oth Bradley, Mark oth Enthalten in Elsevier Science Fitzgerald, Emily ELSEVIER Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study 2020 the international journal for the science and technology of polymers Oxford (DE-627)ELV005093368 volume:226 year:2021 day:4 month:06 pages:0 https://doi.org/10.1016/j.polymer.2021.123840 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.63 Krankenpflege VZ 44.69 Intensivmedizin VZ AR 226 2021 4 0604 0 |
| allfields_unstemmed |
10.1016/j.polymer.2021.123840 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001613.pica (DE-627)ELV054121116 (ELSEVIER)S0032-3861(21)00463-8 DE-627 ger DE-627 rakwb eng 610 VZ 44.63 bkl 44.69 bkl Zhang, Shuo verfasserin aut Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents 2021transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). BODIPY Elsevier Carboxyfluorescein Elsevier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation Elsevier Zhang, Yichuan oth Üçüncü, Muhammed oth Lilienkampf, Annamaria oth Geng, Jin oth Bradley, Mark oth Enthalten in Elsevier Science Fitzgerald, Emily ELSEVIER Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study 2020 the international journal for the science and technology of polymers Oxford (DE-627)ELV005093368 volume:226 year:2021 day:4 month:06 pages:0 https://doi.org/10.1016/j.polymer.2021.123840 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.63 Krankenpflege VZ 44.69 Intensivmedizin VZ AR 226 2021 4 0604 0 |
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10.1016/j.polymer.2021.123840 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001613.pica (DE-627)ELV054121116 (ELSEVIER)S0032-3861(21)00463-8 DE-627 ger DE-627 rakwb eng 610 VZ 44.63 bkl 44.69 bkl Zhang, Shuo verfasserin aut Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents 2021transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). BODIPY Elsevier Carboxyfluorescein Elsevier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation Elsevier Zhang, Yichuan oth Üçüncü, Muhammed oth Lilienkampf, Annamaria oth Geng, Jin oth Bradley, Mark oth Enthalten in Elsevier Science Fitzgerald, Emily ELSEVIER Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study 2020 the international journal for the science and technology of polymers Oxford (DE-627)ELV005093368 volume:226 year:2021 day:4 month:06 pages:0 https://doi.org/10.1016/j.polymer.2021.123840 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.63 Krankenpflege VZ 44.69 Intensivmedizin VZ AR 226 2021 4 0604 0 |
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10.1016/j.polymer.2021.123840 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001613.pica (DE-627)ELV054121116 (ELSEVIER)S0032-3861(21)00463-8 DE-627 ger DE-627 rakwb eng 610 VZ 44.63 bkl 44.69 bkl Zhang, Shuo verfasserin aut Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents 2021transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). BODIPY Elsevier Carboxyfluorescein Elsevier Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation Elsevier Zhang, Yichuan oth Üçüncü, Muhammed oth Lilienkampf, Annamaria oth Geng, Jin oth Bradley, Mark oth Enthalten in Elsevier Science Fitzgerald, Emily ELSEVIER Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study 2020 the international journal for the science and technology of polymers Oxford (DE-627)ELV005093368 volume:226 year:2021 day:4 month:06 pages:0 https://doi.org/10.1016/j.polymer.2021.123840 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.63 Krankenpflege VZ 44.69 Intensivmedizin VZ AR 226 2021 4 0604 0 |
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Enthalten in Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study Oxford volume:226 year:2021 day:4 month:06 pages:0 |
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Enthalten in Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study Oxford volume:226 year:2021 day:4 month:06 pages:0 |
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Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study |
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Zhang, Shuo @@aut@@ Zhang, Yichuan @@oth@@ Üçüncü, Muhammed @@oth@@ Lilienkampf, Annamaria @@oth@@ Geng, Jin @@oth@@ Bradley, Mark @@oth@@ |
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Functional outcomes at 12 months for patients with traumatic brain injury, intracerebral haemorrhage and subarachnoid haemorrhage treated in an Australian neurocritical care unit: A prospective cohort study |
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10.1016/j.polymer.2021.123840 |
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light-controlled, living radical polymerisation mediated by fluorophore-conjugated raft agents |
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Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents |
| abstract |
Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). |
| abstractGer |
Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). |
| abstract_unstemmed |
Photoinduced electron transfer-reversible addition−fragmentation chain-transfer (PET-RAFT) polymerisation allows the controlled synthesis of polymers and provides an alternative to transition metal-based photoinitiators. Here, fluorophore-conjugated RAFT agents, containing either 5-carboxyfluorescein or a “boron-dipyrromethene” (BODIPY) moiety attached to a thiocarbonylthio group, were synthesised. Both agents enabled light-controlled (470 nm, 0.4 mW/cm2) “on/off” polymerisation yielding polymers with a Mw/Mn < 1.50. The BODIPY-based RAFT agent showed excellent photostability and gave polymers that contained a single fluorophore per polymer chain, providing an expedient route to homogeneous fluorescently labelled polymers. This agent was compatible with multiple acrylamide/acrylate monomers with a range of functional groups, with the thiocarbonylthio terminating group enabling further polymer chain extension and the formation of fluorescent block copolymers, as demonstrated by the synthesis of BODIPY-labelled poly(N,N-dimethylacrylamide)-block-poly (3-acrylamidophenyl)boronic acid). |
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Light-controlled, living radical polymerisation mediated by fluorophore-conjugated RAFT agents |
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Zhang, Yichuan Üçüncü, Muhammed Lilienkampf, Annamaria Geng, Jin Bradley, Mark |
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