2021
DOI: 10.1016/j.jorganchem.2021.121681
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Organometallic gold nanoparticles and thin films from cis- and trans-tetrazonium gold(III) salts for electrochemical and photothermal mirror properties

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Cited by 2 publications
(2 citation statements)
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“…Tetrachloroaurate(III) counterions are excellent stabilizers for aryldiazonium cations. 17,[26][27][28][29][30] The preparation of aryldiazonium gold(III) salts is carried out in the presence of tetrachloroauric acid, HAuCl 4 , which provides an acidic medium for the diazotization reaction and also promotes complete dissolution of the aniline precursors to yield ammonium salts. Mohamed, et al protonated 4-aminobenzonitrile with HAuCl 4 in acetonitrile to form the ammonium benzonitrile tetrachloroaurate(III), which was subsequently oxidized using nitrosyl cation to form the diazonium gold(III) salt.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Tetrachloroaurate(III) counterions are excellent stabilizers for aryldiazonium cations. 17,[26][27][28][29][30] The preparation of aryldiazonium gold(III) salts is carried out in the presence of tetrachloroauric acid, HAuCl 4 , which provides an acidic medium for the diazotization reaction and also promotes complete dissolution of the aniline precursors to yield ammonium salts. Mohamed, et al protonated 4-aminobenzonitrile with HAuCl 4 in acetonitrile to form the ammonium benzonitrile tetrachloroaurate(III), which was subsequently oxidized using nitrosyl cation to form the diazonium gold(III) salt.…”
Section: Introductionmentioning
confidence: 99%
“…A major drawback in the use of diazonium salts is their instability, which makes their synthesis, isolation, and purification challenging. However, tetrachloro­aurate­(III) counterions are excellent stabilizers for aryldiazonium cations compared to nonreducible counteranions. , They have shown outstanding stability at room temperature (slowly evolving nitrogen gas over time) and considerable thermal stability. The preparation of aryldiazonium gold­(III) salts is carried out in the presence of tetrachloroauric acid, HAuCl 4 , which provides an acidic medium for the diazotization reaction and also promotes complete dissolution of the aniline precursors to yield ammonium salts.…”
Section: Introductionmentioning
confidence: 99%