indium complexes
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Author(s):  
Dagyum Yoo ◽  
Seong Ho Han ◽  
Sung Kwang Lee ◽  
Taeyong Eom ◽  
Bo Keun Park ◽  
...  

Author(s):  
Myung Hwan Park ◽  
Sang Woo Kwak ◽  
Hanif Mubarok ◽  
Ji Hye Lee ◽  
Hyonseok Hwang ◽  
...  

An approach to the design of highly emissive salen−indium complexes is presented. A series of 4-NR2-appended salen ligands possessing an electron-accepting 1,2-dicyanoethylene bridge and their indium complexes (R = Me...


2021 ◽  
Vol 515 ◽  
pp. 120037
Author(s):  
Nidhi Govil ◽  
Barun Jana
Keyword(s):  

Author(s):  
Hyuk-Joon Jung ◽  
Youngjung Cho ◽  
Diana Kim ◽  
Parisa Mehrkhodavandi

The introduction of cationic charge allows cationic group 13 complexes to be excellent Lewis acid catalysts. Cationic aluminum, gallium, and indium complexes in catalysis are comprehensively reviewed based on the reaction type.


2021 ◽  
Vol 50 (5) ◽  
pp. 1631-1640
Author(s):  
Viviana S. Prado ◽  
Renan C. F. Leitao ◽  
Francisco Silva ◽  
Lurdes Gano ◽  
Isabel C. Santos ◽  
...  

Rapid, low temperature and high yield synthesis of 67Ga and 111In radiocomplexes with new hexadentate bis(semicarbazone) and bis(thiosemicarbazone) chelators.


Molecules ◽  
2020 ◽  
Vol 26 (1) ◽  
pp. 34
Author(s):  
Sang Woo Kwak ◽  
Ju Hyun Hong ◽  
Sang Hoon Lee ◽  
Min Kim ◽  
Yongseog Chung ◽  
...  

A novel class of quinolinol-based dimeric indium complexes (1–6) was synthesized and characterized using 1H and 13C(1H) NMR spectroscopy and elemental analysis. Compounds 1–6 exhibited typical low-energy absorption bands assignable to quinolinol-centered π–π* charge transfer (CT) transition. The emission spectra of 1–6 exhibited slight bathochromic shifts with increasing solvent polarity (p-xylene < tetrahydrofuran (THF) < dichloromethane (DCM)). The emission bands also showed a gradual redshift, with an increase in the electron-donating effect of substituents at the C5 position of the quinoline groups. The absolute emission quantum yields (ΦPL) of compounds 1 (11.2% in THF and 17.2% in film) and 4 (17.8% in THF and 36.2% in film) with methyl substituents at the C5 position of the quinoline moieties were higher than those of the indium complexes with other substituents.


2020 ◽  
Vol 53 (20) ◽  
pp. 8819-8828
Author(s):  
Carlos Diaz ◽  
Tanja Tomković ◽  
Chatura Goonesinghe ◽  
Savvas G. Hatzikiriakos ◽  
Parisa Mehrkhodavandi

2020 ◽  
Vol 40 (3) ◽  
pp. 107-151
Author(s):  
Hira Anwar ◽  
Rosenani A. Haque ◽  
Rahman Shah Zaib Saleem ◽  
Muhammad Adnan Iqbal

AbstractThe indium complexes are being used in many applications like catalysis, optoelectronics, sensors, solar cells, biochemistry, medicine, infrared (IR) mirrors and thin-film transistors (TFTs). In organometallic complexes of indium, it forms different types of complexes with single, double, triple and tetra linkages by coordinating with numerous elements like C, N, O and S and also with some other elements like Se and Ru. So, the present study comprises all the possible ways to synthesize the indium complexes by reacting with different organic ligands; most of them are N-heterocyclic carbenes, amines, amides and phenols. The commonly used solvents for these syntheses are tetrahydrofuran, dichloromethane, toluene, benzene, dimethyl sulfoxide (DMSO) and water. According to the nature of the ligands, indium complexes were reported at different temperatures and stirring time. Because of their unique characteristics, the organometallic chemistry of group 13 metal indium complexes remains a subject of continuing interest in synthetic chemistry as well as material science.


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