Dataset curated

DOI:
https://doi.org/10.34804/supra.20210928315 Cc Cc by 4.0

Title:
Host Properties of Cucurbit[7]uril:  Fluorescence Enhancement of Anilinonaphthalene Sulfonates

https://pubs.acs.org/pb-assets/images/CoverImages_2by1Scaled/jpcbfk-1595795904957.png

Description:
This work describes the fluorescence enhancement of the probes 2,6- and 1,8-ANS via complexation with the macrocyclic host cucurbit[7]uril (Q7). The association of these two guests with the Q7 host has been studied using fluorescence, 1H NMR spectroscopy, and molecular modeling. In the case of 2,6-ANS, 1:1 inclusion complexes are formed via inclusion of the phenyl moiety into the Q7 cavity (as confirmed by NMR), with a large fluorescence enhancement of a factor of 25 ± 3 and an association constant of 600 ± 150 M-1. These values are significantly larger than those reported in the literature for 2,6-ANS inclusion into cucurbit[6]uril (Q6); for example, the association constant is larger by over an order of magnitude, indicating the superior host abilities of Q7 as compared to its smaller homologue. These results are significant, as they provide the first direct comparison of the host abilities of Q6 and Q7. In the case of 1,8-ANS, very large fluorescence enhancement was also observed upon addition of Q7. The enhancement as a function of Q7 concentration indicated the formation of a 2:1 host:guest complex. However, host−guest inclusion was not observed via NMR. Thus, a 2:1 complex where 1,8-ANS is sandwiched between the outer surface of two Q7 molecules is proposed. Such complexation is supported by semiempirical PM3 calculations, and the resulting minimized structures are reminiscent of the structure of the solid exclusion compound of 1,8-ANS and Q6 previously reported in the literature.

Citation:

N. Stojanovic, B. D. Wagner, A. I. Day, R. J. Blanch, SupraBank 2024, Host Properties of Cucurbit[7]uril:  Fluorescence Enhancement of Anilinonaphthalene Sulfonates (dataset). https://doi.org/10.34804/supra.20210928315

Link: https://doi.org/10.34804/supra.20210928315
Export: BibTex | RIS | EndNote
Views Downloads Citations
1555 0 0
Citation:

B. D. Wagner, N. Stojanovic, A. I. Day, R. J. Blanch, J. Phys. Chem. B 2003, 107, 10741–10746.

Link: https://doi.org/10.1021/jp034891j
Export: BibTex | RIS | EndNote |
Creators:
Orcidid | Ror | Brian D. Wagner
Orcidid | Ror | Natasa Stojanovic
Orcidid | Ror | Anthony I. Day
Orcidid | Ror | Rodney J. Blanch

Contributers:
Orcidid | Ror | Changming Hu | DataManager

Included Interactions 3 Info

Show interactions per page
Default trans