Amide-based diarylmaleimide derivatives and polymers: Highly selective and ratiometric fluorescence sensing for anions. (February 2015)
- Record Type:
- Journal Article
- Title:
- Amide-based diarylmaleimide derivatives and polymers: Highly selective and ratiometric fluorescence sensing for anions. (February 2015)
- Main Title:
- Amide-based diarylmaleimide derivatives and polymers: Highly selective and ratiometric fluorescence sensing for anions
- Authors:
- Lin, Zhenghuan
Ma, Yingshuang
Zheng, Xin
Huang, Limei
Yang, E.
Wu, Cheng-Ya
Chow, Tahsin J.
Ling, Qidan - Abstract:
- Abstract: A series of diarylmaleimide derivatives and polymers based on amide group were designed and synthesized to detect anions selectively and sensitively. Three bisindolylmaleimide derivatives (FAM-p, FAM-m and FAM-o) employing trifluoroacetamide as receptor exhibited strong fluorescent quenching upon fluoride and cyanide. Trifluoroacetamide receptor was replaced by acetamide to obtain other two derivatives (AM-p and AM-o) which showed higher selectivity than FAMs with sensing for only fluoride. The diarylmaleimide derivatives were introduced into the backbone of polyfluorene by Suzuki reaction to prepare polymer PFAM and PAM with same sensing selectivity for anions as FAM and AM, respectively. PFAM and PAM were found to be ratiometric fluorescence sensors for a fluorescence resonance energy transfer (FRET) from fluorene segments to diphenylmaleimide units. The experimental and DFT/TDDFT calculation results demonstrated that the interaction mechanism of FAMs with F − and CN − was hydrogen bond interaction and nucleophilic addition reaction, respectively. Graphical abstract: Highlights: The novel fluorescent sensors based on amide showed high selectivity for F − and CN − . The interaction for F − and CN − was hydrogen bond and addition reaction, respectively. The selectivity was improved further by replacing trifluoroacetamide with acetamide. The sensitivity was improved further by introducing sensors into polyfluorene. The copolymers exhibited ratiometric fluorescenceAbstract: A series of diarylmaleimide derivatives and polymers based on amide group were designed and synthesized to detect anions selectively and sensitively. Three bisindolylmaleimide derivatives (FAM-p, FAM-m and FAM-o) employing trifluoroacetamide as receptor exhibited strong fluorescent quenching upon fluoride and cyanide. Trifluoroacetamide receptor was replaced by acetamide to obtain other two derivatives (AM-p and AM-o) which showed higher selectivity than FAMs with sensing for only fluoride. The diarylmaleimide derivatives were introduced into the backbone of polyfluorene by Suzuki reaction to prepare polymer PFAM and PAM with same sensing selectivity for anions as FAM and AM, respectively. PFAM and PAM were found to be ratiometric fluorescence sensors for a fluorescence resonance energy transfer (FRET) from fluorene segments to diphenylmaleimide units. The experimental and DFT/TDDFT calculation results demonstrated that the interaction mechanism of FAMs with F − and CN − was hydrogen bond interaction and nucleophilic addition reaction, respectively. Graphical abstract: Highlights: The novel fluorescent sensors based on amide showed high selectivity for F − and CN − . The interaction for F − and CN − was hydrogen bond and addition reaction, respectively. The selectivity was improved further by replacing trifluoroacetamide with acetamide. The sensitivity was improved further by introducing sensors into polyfluorene. The copolymers exhibited ratiometric fluorescence properties upon F − or CN − . … (more)
- Is Part Of:
- Dyes and pigments. Volume 113(2015)
- Journal:
- Dyes and pigments
- Issue:
- Volume 113(2015)
- Issue Display:
- Volume 113, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 113
- Issue:
- 2015
- Issue Sort Value:
- 2015-0113-2015-0000
- Page Start:
- 129
- Page End:
- 137
- Publication Date:
- 2015-02
- Subjects:
- Amide -- Fluoride -- Cyanide -- Sensor -- Ratiometric fluorescence -- Maleimide
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2014.08.006 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5436.xml