Fatma T Tat's research while affiliated with CUNY Graduate Center and other places
What is this page?
This page lists the scientific contributions of an author, who either does not have a ResearchGate profile, or has not yet added these contributions to their profile.
It was automatically created by ResearchGate to create a record of this author's body of work. We create such pages to advance our goal of creating and maintaining the most comprehensive scientific repository possible. In doing so, we process publicly available (personal) data relating to the author as a member of the scientific community.
If you're a ResearchGate member, you can follow this page to keep up with this author's work.
If you are this author, and you don't want us to display this page anymore, please let us know.
It was automatically created by ResearchGate to create a record of this author's body of work. We create such pages to advance our goal of creating and maintaining the most comprehensive scientific repository possible. In doing so, we process publicly available (personal) data relating to the author as a member of the scientific community.
If you're a ResearchGate member, you can follow this page to keep up with this author's work.
If you are this author, and you don't want us to display this page anymore, please let us know.
Publications (3)
Fullerene coordination ligands bearing one bipyridine or terpyridine unit were synthesized, and their coordination to ruthenium(II) formed linear rod-like donor-acceptor systems. Steady-state fluorescence of [Ru(bpy)(2)(bpy-C(60))](2+) showed a rapid solvent-dependent, intramolecular quenching of the ruthenium(II) MLCT excited state. Time-resolved...
The subject of this paper is a new fullerene building block design with the potential for defined geometry and good electronic communication. The synthesis and characterization of a new pyridinofullerene ligand capable of forming axially symmetric complexes with metalloporphyrins is reported. X-ray structural and molecular modeling studies, (1)H NM...
The synthesis and characterization of a new pyridinofullerene ligand capable of forming axially symmetric complexes with ZnTPP is reported; molecular modelling studies, 1H NMR, UV-Vis spectroscopy and fluorescence quenching data support formation of a strong complex between the new ligand and ZnTPP.
Citations
... These binding constant values were closed to the similar systems 2 and smaller than the fullerene-porphyrin system whose binding force was coordinate bond. 3,4 Also, the steady-state fluorescence spectra titration was utilized by adding C 70 into the MTPP solution (shown in Fig. S17 and S18). The fluorescence of H 2 TPP in the CS 2 solution shows the characteristic emission at 657 nm and 717 nm upon 430 nm excitation. ...
![[object Object]](https://i1.rgstatic.net/ii/profile.image/431912897519618-1479987467453_Q64/Peter-Jarowski-2.jpg)
... Over the last decades covalent functionalization of fullerenes has been extended to include various functionalization reactions 3,19,25-27 , among which the most commonly employed is the Prato reaction for fullerene functionalization through fulleropyrrolidine formation based on the 1,3 dipolar cycloaddition [28][29][30] . As a result, a open Content courtesy of Springer Nature, terms of use apply. ...
... The first fullerene-metal coordination compound was reported in 1998 by Diederich and co-workers, in which the reaction of a dipyridylmethanofullerene with Pt(Et 3 ) 2 (OTf) 2 formed a dimeric fullerene-Pt complex [16]. Although fullerenes modified with terpyridine, bipyridine, dipyrrolidine and pyrazine have been designed and synthesized, the coordination of these fullerene ligands with metal centers only produces discrete coordination complexes [17][18][19][20][21]. The first one-dimensional (1D) MFF was successfully prepared in 2007, wherein a fullerene ligand with two flexible pyridyl donors was synthesized and coordinated with metal ions [7]. ...
