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dc.contributor.authorEl-Zohry, Ahmed
dc.contributor.authorAlturki, Abdullah
dc.contributor.authorYin, Jun
dc.contributor.authorMallick, Arijit
dc.contributor.authorShekhah, Osama
dc.contributor.authorEddaoudi, Mohamed
dc.contributor.authorOoi, Boon S.
dc.contributor.authorMohammed, Omar F.
dc.date.accessioned2019-04-01T11:28:55Z
dc.date.available2019-04-01T11:28:55Z
dc.date.issued2019-02-20
dc.identifier.citationEl-Zohry AM, Alturki A, Yin J, Mallick A, Shekhah O, et al. (2019) Tunable Twisting Motion of Organic Linkers via Concentration and Hydrogen-Bond Formation. The Journal of Physical Chemistry C 123: 5900–5906. Available: http://dx.doi.org/10.1021/acs.jpcc.9b00005.
dc.identifier.issn1932-7447
dc.identifier.issn1932-7455
dc.identifier.doi10.1021/acs.jpcc.9b00005
dc.identifier.urihttp://hdl.handle.net/10754/631784
dc.description.abstractBenzothiadiazole dibenzoic acid (BTDB) derivative is a well-known organic linker in various metal–organic framework structures as well as a fluorescent probe in biological systems. Here, we demonstrate that the radiative and nonradiative decay channels of BTDB can be interplayed and precisely controlled through concentration and hydrogen-bond interactions as directly evidenced experimentally and theoretically. This leads to excited-state structural changes that significantly suppress the torsional motion around the benzothiadiazole moiety, leading to an enormous increase in the emission quantum yields from ∼1 to 70%. These changes are associated with the existence of two equilibria, where dimers and small oligomers form in dimethylformamide (DMF), with high formation constants of 18 000 M–1 and 1.2 × 1013 M–3, respectively. These evolving species, i.e., the dimers and oligomers, are formed via hydrogen bonds between carboxylic acid groups present at the far edge of the rodlike BTDB molecules. The estimated repeating number for this small-oligomer formation via bonded monomers is eight in DMF, as shown by emission spectra analysis. With deprotonation as a control experiment, these associated species can easily collapse with the initial monomer species, confirming the role of the hydrogen-bond formation in the observed phenomena. Theoretical studies and NMR experiments not only confirm the existence of the dimers, but also demonstrate the important role of the hydrogen bonds in the excited-state dynamics. These new findings provide a better understanding of the photophysical behaviors of organic linkers used in a wide range of chemical and biological applications.
dc.description.sponsorshipThe research reported in this publication was supported by funding from King Abdullah University of Science and Technology (KAUST). The authors thank Dr. Jafar Khan for helpful discussions.
dc.publisherAmerican Chemical Society (ACS)
dc.relation.urlhttps://pubs.acs.org/doi/10.1021/acs.jpcc.9b00005
dc.rightsArchived with thanks to Journal of Physical Chemistry C
dc.titleTunable Twisting Motion of Organic Linkers via Concentration and Hydrogen-Bond Formation
dc.typeArticle
dc.contributor.departmentAdvanced Membranes and Porous Materials Research Center
dc.contributor.departmentChemical Science Program
dc.contributor.departmentComputer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division
dc.contributor.departmentElectrical Engineering Program
dc.contributor.departmentFunctional Materials Design, Discovery and Development (FMD3)
dc.contributor.departmentKAUST Solar Center (KSC)
dc.contributor.departmentPhotonics Laboratory
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.contributor.departmentUltrafast Laser Spectroscopy and Four-dimensional Electron Imaging Research Group
dc.identifier.journalThe Journal of Physical Chemistry C
dc.eprint.versionPost-print
kaust.personEl-Zohry, Ahmed
kaust.personAlturki, Abdullah
kaust.personYin, Jun
kaust.personMallick, Arijit
kaust.personShekhah, Osama
kaust.personEddaoudi, Mohamed
kaust.personOoi, Boon S.
kaust.personMohammed, Omar F.
refterms.dateFOA2020-02-20T00:00:00Z
dc.date.published-online2019-02-20
dc.date.published-print2019-03-14


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