2017
DOI: 10.1039/c7ra05049f
|View full text |Cite
|
Sign up to set email alerts
|

Solvent-induced construction of two zinc supramolecular isomers: synthesis, framework flexibility, sensing properties, and adsorption of dye molecules

Abstract: Solvent-induced construction of two zinc supramolecular isomerism, sensing properties and adsorption of dye molecules.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
11
0

Year Published

2017
2017
2022
2022

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 30 publications
(11 citation statements)
references
References 80 publications
0
11
0
Order By: Relevance
“…Solvent suspensions of 1α -DMF exhibit fluorescence intensity in the trend of DMF (424 nm) > ACE (425 nm) ∼ MeOH (420 nm) > DCM (458 nm) > Tol (455 nm) > H 2 O (450 nm), and solvent suspensions of 1β -DMAc show a similar trend of DMF (422 nm) > DCM (464 nm) ∼ DMAc (441 nm) > Tol (461 nm) > H 2 O (463 nm). This is attributed to different collision interactions between the solvent molecules and the frameworks of 1α -DMF and 1β -DMAc. In addition, 1α -DMF in DMF, ACE, and MeOH suspensions and 1β -DMAc in DMF and DMAc suspensions show fluorescence emissions very close to their solid-state fluorescence in position, while, in comparison, both 1α -DMF and 1β -DMAc reveal red shifts more than 20 nm in DCM, Tol, and H 2 O suspensions.…”
Section: Resultsmentioning
confidence: 99%
“…Solvent suspensions of 1α -DMF exhibit fluorescence intensity in the trend of DMF (424 nm) > ACE (425 nm) ∼ MeOH (420 nm) > DCM (458 nm) > Tol (455 nm) > H 2 O (450 nm), and solvent suspensions of 1β -DMAc show a similar trend of DMF (422 nm) > DCM (464 nm) ∼ DMAc (441 nm) > Tol (461 nm) > H 2 O (463 nm). This is attributed to different collision interactions between the solvent molecules and the frameworks of 1α -DMF and 1β -DMAc. In addition, 1α -DMF in DMF, ACE, and MeOH suspensions and 1β -DMAc in DMF and DMAc suspensions show fluorescence emissions very close to their solid-state fluorescence in position, while, in comparison, both 1α -DMF and 1β -DMAc reveal red shifts more than 20 nm in DCM, Tol, and H 2 O suspensions.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, the emission maxima of these suspensions varied from 384 nm to 432 nm, showing remarkable blue shift compared to the solid-state fluorescence. The phenomena can most likely be attributed to the different collision interactions rather than crystal structure change [ 56 , 57 ], since that 1 is highly stable in all chosen solvents. Additionally, it is noted that the fluorescence emission intensities are nearly directly proportional to the concentrations of 1 in H 2 O suspensions ( Figure S4 ).…”
Section: Resultsmentioning
confidence: 99%
“…For other solvent molecules, such as CH 3 OH, CH 3 CN, CH 2 Cl 2 , and toluene, as the dispersion media, MOFs 1 – 5 showed luminescent intensities from moderate to weak. Such phenomena can be mainly attributed to different interactions between the homogeneously dispersible framework structure and distinct solvent molecules [65, 66] . On the other hand, shifts in the luminescence emissions of MOFs 1 – 5 were observed upon changing the solvent, with the longest luminescence band appearing in the case of toluene ( λ em =446–460 nm).…”
Section: Resultsmentioning
confidence: 99%