195062-59-0Relevant articles and documents
Naphthalimide-based fluorescent nanoprobes for the detection of saccharides
Qiao, Zichun,Chen, Zhaoyang,Zhang, Shuo,Cui, Zepeng,Xu, Zhuoran,Zhang, Weibing,Qian, Junhong
, p. 16428 - 16435 (2018)
Three kinds of fluorescent nano probes SN-A, SN-B and SN-C, based on the photo-induced electron transfer mechanism, were synthesized for the detection of saccharides, in which small fluorescent probes with 1,8-naphthalimide as the fluorophore and phenylboronic acid as the receptor were covalently bound to SiO2 nanoparticles. The fluorescent nano particles were characterized by TEM, IR, UV-Vis and fluorescence spectra. The results showed that the particle diameter exerted a significant influence on the performance of the nanoprobes; however, the length of the linker affected the spectral response to a much lesser extent. The fluorescence intensity at 530 nm (I530) of SN-B exhibited a good linear relationship with the fructose/sorbitol concentration and was employed in the detection of the fructose content in drinks.
Mononuclear Copper(I) complexes based on phenanthroline derivatives P^N^N^P tetradentate ligands: Syntheses, crystal structure, photochemical properties
Chen, Hao,Xu, Liang-Xuan,Yan, Li-Juan,Liu, Xue-Fen,Xu, Dan-Dan,Yu, Xiao-Cong,Fan, Jin-Xuan,Wu, Qing-An,Luo, Shu-Ping
, (2020)
Two novel heteroleptic Cu(I) complexes with the single tetradentate ligands have been designed and synthesized from phenanthroline. The complexes having one copper structure were fully characterized by NMR, ESI-MS and the single-crystal X-ray structures. Their photoelectric chemical properties were investigated by using cyclic voltammetry, UV/vis and fluorescence spectroscopy. Compared with the classic Cu(P^P)(N^N) complexes, this distorted tetrahedral coordination structure of Cu(P^N^N^P) complexes showed a wider excitation wavelength and a red-shifted about 100 nm emission peak, due to the link function between phenanthroline and phosphorus ligands. Moreover, the copper complex B having the naphthyl link groups displayed high red-emissive photoluminescence quantum efficiency (PLQY), which was up to 3.8%.
Photochemical and electrochemical C-N borylation of arylhydrazines
Du, Linlin,Sun, Li,Zhang, Hua
supporting information, p. 1716 - 1719 (2022/02/21)
The C-N borylation of arylhydrazine hydrochlorides with bis(pinacolato)diboron was achieved under photochemical and electrochemical conditions, respectively. This novel and scalable transformation provides two efficient and mild transition-metal-free synt
Palladium-catalyzed borylation of aryl bromides and chlorides using phosphatrioxa-adamantane ligands
Lamola, Jairus L.,Moshapo, Paseka T.,Holzapfel, Cedric W.,Christopher Maumela, Munaka
supporting information, (2021/12/13)
Catalysts based on the combination of Pd(OAc)2 and the electron-deficient phosphatrioxa-adamantane ligands are described for borylation of aryl bromides and chlorides. Catalytic evaluation of a small library of phosphatrioxa-adamantane ligands provided some insights on the preferred ligand steric profile for borylation reactions. The corresponding aryl boronate esters were accessed under mild conditions (25–70 °C) and isolated in high yields (up to 96%).
Cross-Coupling through Ag(I)/Ag(III) Redox Manifold
Demonti, Luca,Mézailles, Nicolas,Nebra, Noel,Saffon-Merceron, Nathalie
supporting information, p. 15396 - 15405 (2021/10/12)
In ample variety of transformations, the presence of silver as an additive or co-catalyst is believed to be innocuous for the efficiency of the operating metal catalyst. Even though Ag additives are required often as coupling partners, oxidants or halide scavengers, its role as a catalytically competent species is widely neglected in cross-coupling reactions. Most likely, this is due to the erroneously assumed incapacity of Ag to undergo 2e? redox steps. Definite proof is herein provided for the required elementary steps to accomplish the oxidative trifluoromethylation of arenes through AgI/AgIII redox catalysis (i. e. CEL coupling), namely: i) easy AgI/AgIII 2e? oxidation mediated by air; ii) bpy/phen ligation to AgIII; iii) boron-to-AgIII aryl transfer; and iv) ulterior reductive elimination of benzotrifluorides from an [aryl-AgIII-CF3] fragment. More precisely, an ultimate entry and full characterization of organosilver(III) compounds [K]+[AgIII(CF3)4]? (K-1), [(bpy)AgIII(CF3)3] (2) and [(phen)AgIII(CF3)3] (3), is described. The utility of 3 in cross-coupling has been showcased unambiguously, and a large variety of arylboron compounds was trifluoromethylated via [AgIII(aryl)(CF3)3]? intermediates. This work breaks with old stereotypes and misconceptions regarding the inability of Ag to undergo cross-coupling by itself.
