Aggregation induced emission based fluorenes as dual-channel fluorescent probes for rapid detection of cyanide: applications of smartphones and logic gates. Issue 29 (29th June 2022)
- Record Type:
- Journal Article
- Title:
- Aggregation induced emission based fluorenes as dual-channel fluorescent probes for rapid detection of cyanide: applications of smartphones and logic gates. Issue 29 (29th June 2022)
- Main Title:
- Aggregation induced emission based fluorenes as dual-channel fluorescent probes for rapid detection of cyanide: applications of smartphones and logic gates
- Authors:
- Majeed, Shumaila
Waseem, Muhammad Tahir
Junaid, Hafiz Muhammad
Khan, Gul Shahzada
Nawazish, Shamyla
Mahmood, Tariq
Khan, Asad Muhammad
Shahzad, Sohail Anjum - Abstract:
- Abstract : Rational modification of molecular structure by incorporating electron donating groups can play a potential role for designing aggregation induced emission (AIE) active fluorescent probes. Abstract : Rational modification of molecular structure by incorporating electron donating groups can play a potential role for designing aggregation induced emission (AIE) active fluorescent probes. Based on this principle, fluorescent probes (1a–c ) were synthesized, and they displayed excellent aggregation induced emission (AIE) behavior in a H2 O/DMF (4 : 1, v / v ) mixture due to restrictions in intramolecular charge transfer (ICT). As a comparison, probe 1d was synthesized by installing an electron withdrawing (–NO2 ) group that surprisingly quenched the aggregation behaviour. Additionally, AIE active probes 1a–c displayed a highly sensitive dual channel (fluorometric and colorimetric) response towards rapid detection of CN −, which is an active toxic material. Probes 1a–c showed selectively enhanced fluorescence emission behavior towards CN − with detection limits of 1.34 ppb, 1.38 ppb, and 1.54 ppb, respectively. The sensing mechanism involves Michael type adduct formation due to the nucleophilic addition reaction of cyanide with probes and was confirmed through 1 H NMR titration experiments. In contrast, probe 1d containing an electron withdrawing moiety showed insensitivity towards CN − . Therefore, this study provides the efficient strategy to induce AIE character inAbstract : Rational modification of molecular structure by incorporating electron donating groups can play a potential role for designing aggregation induced emission (AIE) active fluorescent probes. Abstract : Rational modification of molecular structure by incorporating electron donating groups can play a potential role for designing aggregation induced emission (AIE) active fluorescent probes. Based on this principle, fluorescent probes (1a–c ) were synthesized, and they displayed excellent aggregation induced emission (AIE) behavior in a H2 O/DMF (4 : 1, v / v ) mixture due to restrictions in intramolecular charge transfer (ICT). As a comparison, probe 1d was synthesized by installing an electron withdrawing (–NO2 ) group that surprisingly quenched the aggregation behaviour. Additionally, AIE active probes 1a–c displayed a highly sensitive dual channel (fluorometric and colorimetric) response towards rapid detection of CN −, which is an active toxic material. Probes 1a–c showed selectively enhanced fluorescence emission behavior towards CN − with detection limits of 1.34 ppb, 1.38 ppb, and 1.54 ppb, respectively. The sensing mechanism involves Michael type adduct formation due to the nucleophilic addition reaction of cyanide with probes and was confirmed through 1 H NMR titration experiments. In contrast, probe 1d containing an electron withdrawing moiety showed insensitivity towards CN − . Therefore, this study provides the efficient strategy to induce AIE character in fluorescent probes and expands the mechanistic approach toward the sensing of toxic CN − . … (more)
- Is Part Of:
- RSC advances. Volume 12:Issue 29(2022)
- Journal:
- RSC advances
- Issue:
- Volume 12:Issue 29(2022)
- Issue Display:
- Volume 12, Issue 29 (2022)
- Year:
- 2022
- Volume:
- 12
- Issue:
- 29
- Issue Sort Value:
- 2022-0012-0029-0000
- Page Start:
- 18897
- Page End:
- 18910
- Publication Date:
- 2022-06-29
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2ra03119a ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22261.xml