Cucurbit[6]uril-based carbon dots for recognizing l-tryptophan and capecitabine. (24th August 2022)
- Record Type:
- Journal Article
- Title:
- Cucurbit[6]uril-based carbon dots for recognizing l-tryptophan and capecitabine. (24th August 2022)
- Main Title:
- Cucurbit[6]uril-based carbon dots for recognizing l-tryptophan and capecitabine
- Authors:
- Liu, Ming
Cen, Ran
Lu, Ji-Hong
Meng, Tie-Hong
Li, Chun-Rong
Redshaw, Carl
Prior, Timothy J.
Tao, Zhu
Xiao, Xin - Abstract:
- Abstract : Fluorescent nitrogen and fluorine doped carbon dots (CDs) were prepared by a hydrothermal method using levofloxacin (LVFX) and cucurbit[6]uril (Q[6]) as the nitrogen and carbon sources, respectively. Abstract : Fluorescent nitrogen and fluorine doped carbon dots (CDs) were prepared by a hydrothermal method using levofloxacin (LVFX) and cucurbit[6]uril (Q[6]) as the nitrogen and carbon sources, respectively. Decomposition of LVFX occurred at elevated temperature affording N, N ′-desethylene levofloxacin hydrochloride ( N, N ′-DLH). The crystal structure of the resulting inclusion complex N, N ′-DLH@Q[6]·[CdCl4 ]2 (H3 O)·9H2 O was determined, where N, N ′-DLH is protonated on each of the terminal nitrogens and the quinone functionality is a quinol which forms an intramolecular hydrogen bond to the carboxylic acid. The synthesized N, N ′-DLH containing Q[6]-CDs emitted intense blue fluorescence with high photostability and exhibited stability at high ionic strength. In particular, the original rigid macrocyclic skeletons of these hosts were retained during the fabrication process, which helps in uniquely distinguishing them from other reported CDs. Meanwhile, the performance of the Q[6]-CDs was characterized using fluorescence and NMR spectroscopies. Subsequently, using the obtained Q[6]-CDs, an efficient sensing method for l -tryptophan (l -Trp) and capecitabine (CAP) has been developed based on macrocyclic host–guest chemistry. Under applicable conditions, theAbstract : Fluorescent nitrogen and fluorine doped carbon dots (CDs) were prepared by a hydrothermal method using levofloxacin (LVFX) and cucurbit[6]uril (Q[6]) as the nitrogen and carbon sources, respectively. Abstract : Fluorescent nitrogen and fluorine doped carbon dots (CDs) were prepared by a hydrothermal method using levofloxacin (LVFX) and cucurbit[6]uril (Q[6]) as the nitrogen and carbon sources, respectively. Decomposition of LVFX occurred at elevated temperature affording N, N ′-desethylene levofloxacin hydrochloride ( N, N ′-DLH). The crystal structure of the resulting inclusion complex N, N ′-DLH@Q[6]·[CdCl4 ]2 (H3 O)·9H2 O was determined, where N, N ′-DLH is protonated on each of the terminal nitrogens and the quinone functionality is a quinol which forms an intramolecular hydrogen bond to the carboxylic acid. The synthesized N, N ′-DLH containing Q[6]-CDs emitted intense blue fluorescence with high photostability and exhibited stability at high ionic strength. In particular, the original rigid macrocyclic skeletons of these hosts were retained during the fabrication process, which helps in uniquely distinguishing them from other reported CDs. Meanwhile, the performance of the Q[6]-CDs was characterized using fluorescence and NMR spectroscopies. Subsequently, using the obtained Q[6]-CDs, an efficient sensing method for l -tryptophan (l -Trp) and capecitabine (CAP) has been developed based on macrocyclic host–guest chemistry. Under applicable conditions, the detection limits for l -Trp and CAP were calculated to be 5.13 × 10 −8 M and 1.48 × 10 −8 M, respectively. … (more)
- Is Part Of:
- Materials chemistry frontiers. Volume 6:Number 19(2022)
- Journal:
- Materials chemistry frontiers
- Issue:
- Volume 6:Number 19(2022)
- Issue Display:
- Volume 6, Issue 19 (2022)
- Year:
- 2022
- Volume:
- 6
- Issue:
- 19
- Issue Sort Value:
- 2022-0006-0019-0000
- Page Start:
- 2859
- Page End:
- 2868
- Publication Date:
- 2022-08-24
- Subjects:
- Materials science -- Periodicals
Chemistry -- Periodicals
540 - Journal URLs:
- http://www.rsc.org/journals-books-databases/about-journals/materials-chemistry-frontiers/ ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2qm00589a ↗
- Languages:
- English
- ISSNs:
- 2052-1529
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5394.107200
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