Fabrication of a "turn-on"-type enantioselective fluorescence sensor via a modified achiral MOF: applications for synchronous detection of phenylalaninol enantiomers. Issue 3 (26th November 2020)
- Record Type:
- Journal Article
- Title:
- Fabrication of a "turn-on"-type enantioselective fluorescence sensor via a modified achiral MOF: applications for synchronous detection of phenylalaninol enantiomers. Issue 3 (26th November 2020)
- Main Title:
- Fabrication of a "turn-on"-type enantioselective fluorescence sensor via a modified achiral MOF: applications for synchronous detection of phenylalaninol enantiomers
- Authors:
- Xiao, Jiannan
Wang, Xueling
Xu, Xuebin
Tian, Fuli
Liu, Zhiliang - Abstract:
- Abstract : One pair of homochiral UiO-66 analogues, S -1 and R -1, can detect enantiomeric PA with different ef values and a distinct enantioselectivity factor α . Abstract : Homochiral metal–organic frameworks (HMOFs) have garnered considerable attention due to their extrachiral properties and broad application for chiral recognition. However, assembling a pair of high-quality chiral MOFs for sensing enantiomers precisely is a formidable challenge because of the complicated chiral environment and uncontrollable coordinated conditions. Herein, one pair of homochiral UiO-66 analogues, S -1 (l -AP@UiO-66-(COOH)2 ) and R -1 (d -AP@UiO-66-(COOH)2 ), are reported for chiral recognition. They were fabricated via a condensation reaction between the carboxyl groups of UiO-66-(COOH)2 and amino groups of l /d -amino propanol (l /d -AP). These novel fluorescent probes exhibited highly enantioselective fluorescence enhancement towards l /d -phenylalaninol (l /d -PA). For example, when S -1 and R -1 were treated with l -PA or d -PA, they displayed different fluorescence responses: the enantiomeric fluorescence enhancement ratio (ef) was 2.51 and 0.41 for S -1 and R -1, respectively. Hence, a visible difference in fluorescence enhancement for l -PA and d -PA and excellent enantioselective behavior between S -1 and l -PA (or R -1 and d -PA) was displayed. Measurements of fluorescence lifetime, powder X-ray diffraction, molecular-dynamic simulations and Benesi–Hildebrand plots were employedAbstract : One pair of homochiral UiO-66 analogues, S -1 and R -1, can detect enantiomeric PA with different ef values and a distinct enantioselectivity factor α . Abstract : Homochiral metal–organic frameworks (HMOFs) have garnered considerable attention due to their extrachiral properties and broad application for chiral recognition. However, assembling a pair of high-quality chiral MOFs for sensing enantiomers precisely is a formidable challenge because of the complicated chiral environment and uncontrollable coordinated conditions. Herein, one pair of homochiral UiO-66 analogues, S -1 (l -AP@UiO-66-(COOH)2 ) and R -1 (d -AP@UiO-66-(COOH)2 ), are reported for chiral recognition. They were fabricated via a condensation reaction between the carboxyl groups of UiO-66-(COOH)2 and amino groups of l /d -amino propanol (l /d -AP). These novel fluorescent probes exhibited highly enantioselective fluorescence enhancement towards l /d -phenylalaninol (l /d -PA). For example, when S -1 and R -1 were treated with l -PA or d -PA, they displayed different fluorescence responses: the enantiomeric fluorescence enhancement ratio (ef) was 2.51 and 0.41 for S -1 and R -1, respectively. Hence, a visible difference in fluorescence enhancement for l -PA and d -PA and excellent enantioselective behavior between S -1 and l -PA (or R -1 and d -PA) was displayed. Measurements of fluorescence lifetime, powder X-ray diffraction, molecular-dynamic simulations and Benesi–Hildebrand plots were employed to determine the observed high enantioselectivity for l /d -PA. In brief, we found that two post-modified HMOFs, S -1 and R -1, were outstanding enantioselective sensors for detecting l -PA and d -PA. They had a prominent difference in ef and remarkable enantioselectivity factor α and ΔΔ G based on steric hindrance and stereochemical difference. … (more)
- Is Part Of:
- Analyst. Volume 146:Issue 3(2021)
- Journal:
- Analyst
- Issue:
- Volume 146:Issue 3(2021)
- Issue Display:
- Volume 146, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 146
- Issue:
- 3
- Issue Sort Value:
- 2021-0146-0003-0000
- Page Start:
- 937
- Page End:
- 942
- Publication Date:
- 2020-11-26
- Subjects:
- Chemistry, Analytic -- Periodicals
543 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/an?e=1#!issueid=an139020&type=current&issnprint=0003-2654 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0an01879a ↗
- Languages:
- English
- ISSNs:
- 0003-2654
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0893.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15849.xml