نتایج جستجو برای: uv vis and fluorescence spectroscopies

تعداد نتایج: 16857933  

2018
Baris Temelli Hilal Kalkan

The preparation of β-meso directly linked porphyrin-corrole hybrids was realized for the first time via an InCl3-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by 1H NMR, 13C NMR, 2D NMR, UV-vis absorption and fluorescence spectroscopy.

Journal: :Chemical communications 2009
Joseph J Peterson Yoan C Simon E Bryan Coughlin Kenneth R Carter

Polyfluorene with p-carborane in the backbone was synthesized from the new monomer 1,12-bis(7-bromo-9,9-dihexyl-9H-fluoren-2-yl)-closo-1,12-dicarbodecaborane to give a high MW, soluble, blue-emitting material characterized by NMR, UV-vis, and fluorescence spectroscopy.

2016
Tian Li Zhengjun Cheng Lijun Cao Xiaohui Jiang Lei Fan

In this data article, the fluorescence, UV-vis absorption and FTIR spectra data of BSA-AR1/AG50 system were presented, which were used for obtaining the binding characterization (such as binding constant, binding distance, binding site, thermodynamics, and structural stability of protein) between BSA and AR1/AG50.

2016
Julia Meihua Tan Govindarajan Karthivashan Shafinaz Abd Gani Sharida Fakurazi Mohd Zobir Hussein

In this paper, we demonstrate the preparation of silibinin-loaded carbon nanotubes (SWSB) with surface coating agents via non-covalent approach as an effective drug delivery system. The resulting surface-coated SWSB nanocomposites are extensively characterized by Fourier transform infrared (FTIR) and Raman spectroscopies, ultraviolet-visible (UV-Vis) spectrometry and field emission scanning ele...

Journal: :Dalton transactions 2016
Satoru Mori Naoya Ogawa Etsuko Tokunaga Seiji Tsuzuki Norio Shibata

An unsymmetrical subphthalocyanine trimer consisting of three different subphthalocyanine units was synthesized. Its optical and physical properties were investigated by UV/Vis, fluorescence spectrometry, cyclic voltammetry and computations. Energy transfer from the non-substituted subphthalocyanine unit to the perfluorinated subphthalocyanine unit via a trifluoroethoxy substituted unit is sugg...

Journal: :Organic & biomolecular chemistry 2008
Hideyuki Yoshiyama Norio Shibata Takefumi Sato Shuichi Nakamura Takeshi Toru

A novel covalently linked binuclear phthalocyanine 1 was synthesized by the "double-click" reaction. The UV-vis and fluorescence spectra and electrochemistry revealed that the geometry of 1 is a closed clamshell conformation in which a strong electronic interaction is observed between the two Pc moieties.

Journal: :Chemosensors 2022

We present the synthesis and analytical, spectroscopic computational characterization of three amino-substituted benzo[b]thieno[2,3-b]pyrido[1,2-a]benzimidazoles as novel pH probes with a potential application in pH-sensing materials. The designed systems differ number position introduced isobutylamine groups on pentacyclic aromatic core, which affects their photophysical acid-base properties. ...

2014

There are specifi c benefi ts to using a UV-Vis spectrophotometer with diode array detector technology compared to those offered when using traditional scanning UV-Vis instruments. Within the molecular spectroscopy group, Agilent is able to offer both types of UV-Vis instruments. The Agilent Cary 60 UV-Vis, based on Xenon fl ash lamp technology, is the ideal scanning instrument for many routine...

Journal: :Chemical communications 2010
Marc Lepeltier Olena Lukoyanova Alex Jacobson Shehzad Jeeva Dmitrii F Perepichka

A new class of heteroacenes containing B, N and S elements in the 22-electron aromatic nucleus has been synthesized by reaction of diaminoterthiophenes with dichlorophenylborane. Their structure was studied by X-ray crystallography and DFT calculations. UV-Vis absorption /emission spectroscopy shows high rigidity and deep-blue fluorescence of these compounds.

Journal: :Organic & biomolecular chemistry 2011
Tomoharu Tanikawa Masaichi Saito Jing Dong Guo Shigeru Nagase

Novel trisilasumanenes that have no substituents on the exo carbon atoms, silicon analogues of sumanene, were prepared via repetitive lithiations of triphenylene followed by introduction of silicon functionalities. The optical properties of these trisilasumanenes and their related compounds were investigated by UV-vis and fluorescence spectroscopy.

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