Octupolar Acrylonitrile‐Bridged 2D‐Conjugated Polymers Enable Bright Far‐Red Emission with Intense Two‐Photon Absorption via Alkoxylation Chemistry. Issue 36 (28th July 2021)
- Record Type:
- Journal Article
- Title:
- Octupolar Acrylonitrile‐Bridged 2D‐Conjugated Polymers Enable Bright Far‐Red Emission with Intense Two‐Photon Absorption via Alkoxylation Chemistry. Issue 36 (28th July 2021)
- Main Title:
- Octupolar Acrylonitrile‐Bridged 2D‐Conjugated Polymers Enable Bright Far‐Red Emission with Intense Two‐Photon Absorption via Alkoxylation Chemistry
- Authors:
- Mo, Chunshao
Yang, Meijia
Cheng, Zhixue
Tang, Xikang
Yang, Lifen
Su, Ruonan
Li, Jing
Feng, Jiangshan
Fang, Long
Yang, Kexin
Chen, Zhuanggui
Yu, Dingshan - Abstract:
- Abstract: Herein, alkoxylation chemistry is introduced as a "one‐stone‐three‐birds" solution for exploring a new family of highly‐fluorescent octupolar 2D‐conjugated organic polymers/frameworks (OCOPs/OCOFs) combining far‐red emission, high fluorescence quantum yield (QY), and strong two‐photon absorption (TPA). Both alkoxy‐substituted OCOP and OCOF comprising acrylonitrile‐bridged strongly‐coupled donor3‐(acceptor core) chromophores densely packed in either disordered or ordered forms, exhibit significantly redshifted emission. They produce high QY of 22.2% and 27.8% in tetrahydrofuran, large TPA cross section of 600 and 1124 GM, and 2–3 folds and 15–30 folds that of non‐alkoxylate amorphous counterpart respectively. Combined theoretical and experimental studies reveal unique "one‐stone‐three‐birds" role of the alkoxylation in realizing red‐shifted‐emission, improved QY and TPA enabled by inducing steric hindrance effect for weakened π–π stacking, and triggering p–π conjugation effect for electronically engineering octupolar chromophores, while the crystalline engineering enables enforced coplanarity conformation and improved π–electron delocalization for further improved QY and TPA. The robust and biocompatible pentoxy‐substituted polymer can be used not only as metal‐free red‐emissive phosphor for efficient warm white light‐emitting diodes, but also as efficient two‐photon fluorescence probes for bio‐imaging. Abstract : A "one‐stone‐three‐birds" alkoxylation solution isAbstract: Herein, alkoxylation chemistry is introduced as a "one‐stone‐three‐birds" solution for exploring a new family of highly‐fluorescent octupolar 2D‐conjugated organic polymers/frameworks (OCOPs/OCOFs) combining far‐red emission, high fluorescence quantum yield (QY), and strong two‐photon absorption (TPA). Both alkoxy‐substituted OCOP and OCOF comprising acrylonitrile‐bridged strongly‐coupled donor3‐(acceptor core) chromophores densely packed in either disordered or ordered forms, exhibit significantly redshifted emission. They produce high QY of 22.2% and 27.8% in tetrahydrofuran, large TPA cross section of 600 and 1124 GM, and 2–3 folds and 15–30 folds that of non‐alkoxylate amorphous counterpart respectively. Combined theoretical and experimental studies reveal unique "one‐stone‐three‐birds" role of the alkoxylation in realizing red‐shifted‐emission, improved QY and TPA enabled by inducing steric hindrance effect for weakened π–π stacking, and triggering p–π conjugation effect for electronically engineering octupolar chromophores, while the crystalline engineering enables enforced coplanarity conformation and improved π–electron delocalization for further improved QY and TPA. The robust and biocompatible pentoxy‐substituted polymer can be used not only as metal‐free red‐emissive phosphor for efficient warm white light‐emitting diodes, but also as efficient two‐photon fluorescence probes for bio‐imaging. Abstract : A "one‐stone‐three‐birds" alkoxylation solution is introduced for developing a new class of highly‐fluorescent, acrylonitrile‐bridged, and octupolar 2D conjugated polymers/frameworks with far‐red emission, high quantum yield, and large two‐photon absorption cross section simultaneously, demonstrating versatile uses for warm white light‐emitting diodes and in vitro/vivo bioimaging. … (more)
- Is Part Of:
- Small. Volume 17:Issue 36(2021)
- Journal:
- Small
- Issue:
- Volume 17:Issue 36(2021)
- Issue Display:
- Volume 17, Issue 36 (2021)
- Year:
- 2021
- Volume:
- 17
- Issue:
- 36
- Issue Sort Value:
- 2021-0017-0036-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-07-28
- Subjects:
- 2D‐conjugated polymers -- alkoxylation chemistry -- donor‐acceptor -- far‐red fluorescence -- two‐photon absorption
Nanotechnology -- Periodicals
Nanoparticles -- Periodicals
Microtechnology -- Periodicals
620.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1613-6829 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/smll.202100955 ↗
- Languages:
- English
- ISSNs:
- 1613-6810
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- 18930.xml