Kinetically stabilized congeners of carbenes, R C, possessing six valence electrons (four bonding electrons and two non-bonding electrons) have been restricted to Group 14 elements, R E (E=Si, Ge, Sn, Pb; R=alkyl or aryl) whereas isoelectronic Group 15 cations, divalent species of type [R E] (E=P, As, Sb, Bi; R=alkyl or aryl), were unknown. Herein, we report the first two examples, namely the bismuthenium ion [(2,6-Mes C H ) Bi][BAr ] (1; Mes=2,4,6-Me C H , Ar =3,5-(CF ) C H ) and the stibenium ion [(2,6-Mes C H ) Sb][B(C F ) ] (2), which were obtained by using a combination of bulky meta-terphenyl substituents and weakly coordinating anions.
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http://dx.doi.org/10.1002/anie.201803160 | DOI Listing |
Sci Adv
November 2024
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China.
As versatile ligands with extraordinary coordination capabilities, RPH (R = alkyl or aryl) are rarely used in constructing metal nanoclusters due to their volatility, toxicity, spontaneous flammability, and susceptibility to oxidation. In this work, we designed a primary and tertiary phosphorus-bound diphosphine chelator (2-PhPCHPH) to create ultrastable silver nanoclusters with metallic aromaticity. By controlling the deprotonation rate of 2-PhPCHPH and adjusting the templates, we successfully synthesized two near-infrared emissive nanoclusters, and , which have analogous icosidodecahedral Ag shells with an symmetry.
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.
J Am Chem Soc
August 2024
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education; Yunnan Key Laboratory of Research and Development for Natural Products; School of Pharmacy, Yunnan University, Kunming 650500, P. R. China.
Stereochemically pure saccharides have indispensable roles in fields ranging from medicinal chemistry to materials science and organic synthesis. However, the development of a simple, stereoselective, and efficient glycosylation protocol to access α- and β-C-glycosides (particularly 2-deoxy entities) remains a persistent challenge. Existing studies have primarily focused on C1 modification of carbohydrates and transformation of glycosyl radical precursors.
View Article and Find Full Text PDFDalton Trans
August 2024
Department of Chemistry and Department of Biophysics, University of Michigan, Ann Arbor, MI 48109, USA.
Molecules
October 2023
Departamento de Química Inorgánica, Universidade de Vigo, Campus Universitario, 36310 Vigo, Spain.
Organic amines are important compounds present in a wide variety of products, which makes the development of new systems for their detection an interesting field of study. New organometallic complexes of group 9 [MCp*X(2'-R-2-py-SBF)] (M = Ir, Rh; R = H, X = Cl (), R = H, X = OAc (), R = CHO, X = Cl ()), and [IrCp*Cl(2', 7-diCHO-2-py-SBF)] () (Cp* pentamethylcyclopentadienyl, SBF = 9,9'-spirobifluorene) bearing bidentate C-N ligands based on 9,9'-spirobifluorene were obtained and characterized by NMR spectroscopy, mass spectrometry, IR spectroscopy, and X-ray diffraction analysis when possible. The formation of a Schiff base to give complexes with the formula [MCp*Cl(2'-CH=NR-2-py-SBF)] (M = Ir, Rh; R = alkyl or aryl (-)), through condensation of an amine, and the aldehyde group present in these new complexes was studied leading to a selective reactivity depending on the nature of the amine and the metal center.
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