173681-56-6Relevant articles and documents
Ir(III) complex-based phosphorescence and electrochemiluminescence chemodosimetric probes for Hg(II) ions with high selectivity and sensitivity
Rhee, Hayoung,Kim, Taemin,Hong, Jong-In
, p. 3803 - 3810 (2018)
Mercury, one of the most prevalent toxic metal elements, poses severe risks to human health and the environment. Several molecular probes have been developed for colorimetric and fluorometric detection of Hg(ii) ions. Nevertheless, development of a rapid, selective, and sensitive probe for Hg(ii) ions remains important. Herein, we report three Ir(iii) complex-based phosphorescence and electrochemiluminescence chemodosimeters for the selective detection of Hg(ii) ions. The acetylacetonate ancillary ligand of probe 1 reacts selectively with the Hg(ii) ion, inducing phosphorescence enhancement with a concomitant blue-shift. Meanwhile, the Hg(ii) ion selectively quenches the phosphorescence of probe 2. Probes 1 and 2 showed low detection limits (LOD) of 73 and 160 nM, respectively. In addition, the Hg(ii) ion level was successfully monitored by the electrochemiluminescence decrement of probe 9 with a good linear correlation between 0 and 40 μM, with a detection limit of 170 pM.
Cp*Rh(iii)/boron hybrid catalysis for directed C-H addition to β-substituted α,β-unsaturated carboxylic acids
Hirata, Yuki,Kojima, Masahiro,Matsunaga, Shigeki,Tanaka, Ryo,Yoshino, Tatsuhiko
supporting information, p. 76 - 79 (2021/12/29)
The C-H bond addition reaction of 2-phenylpyridine derivatives with α,β-unsaturated carboxylic acids catalyzed by Cp*Rh(iii)/BH3·SMe2is reported. Activation of C-H bonds with the rhodium catalyst and activation of α,β-unsaturated carboxylic acids with the boron catalyst cooperatively work, and a BINOL-urea hybrid ligand significantly improved the reactivity. With the optimized hybrid catalytic system, various β-disubstituted carboxylic acids were obtained under mild reaction conditions.
Magnetic chitosan-functionalized cobalt-NHC: Synthesis, characterization and catalytic activity toward Suzuki and Sonogashira cross-coupling reactions of aryl chlorides
Hajipour, Abdol R.,Malek, Shaghayegh Sadeghi
, (2021/04/23)
Aryl chlorides are one of the most stable and available electrophiles, however, their coupling with nucleophiles remains a challenge in organic synthesis. Herein, we prepared a Cobalt-NHC (N-Heterocyclic carbene) complex anchored on magnetic chitosan nanoparticles and assayed its catalytic activity for the reactions of substituted phenylboronic acid and also phenlacetylene with derivatives of aryl chlorides. These reactions are of great importance since they are employed for the synthesis of unsymmetrical diarylethynes and biphenyls, which belong to a prime class of building blocks. The synthesized nanocatalyst was found to be highly efficient in Suzuki and Sonogashira coupling in terms of their activity and recyclability in polyethylene glycol (PEG) as a green reaction media under conditions of temperatures (70 and 100 °C) and Co loading (3 and 6 mol%). To the best of our knowledge, this is the first attempt of using cobalt-NHC complex for catalyzing the abovementioned reactions. Moreover, replacing the earth-abundant Cobalt-based catalyst as an alternative to high cost palladium make this approach promising from sustainable chemistry view.
Biaryl Cross-Coupling Enabled by Photo-Induced Electron Transfer
Hayashi, Hirohito,Wang, Bin,Wu, Xiangyang,Teo, Shi Jie,Kaga, Atsushi,Watanabe, Kohei,Takita, Ryo,Yeow, Edwin K. L.,Chiba, Shunsuke
supporting information, p. 2223 - 2231 (2020/04/30)
We report a protocol for aryl cross-coupling of electron-deficient aryl halides with electron-rich (hetero)arenes that is driven solely by violet light. This process takes advantage of formation of photo-excited state of electron-deficient aryl halides, that are reduced by electron-rich (hetero)arenes to form a pair of aryl anion and cation radicals. The resulting aryl anion radicals of aryl halides undergo mesolysis of the carbon-halogen bond to generate aryl radicals, that are coupled most likely with aryl cation radicals to afford functionalized biaryls. (Figure presented.).
