Adducts of Bicyclic (Alkyl)(Amino)Carbene with ECl3 and Three Electron Reduction Thereof: Syntheses of BICAAC Stabilized E−E Bonded Compounds (E=P, Sb)
Abstract:The stoichiometric reaction of bicyclic (alkyl)(amino)carbene (BICAAC) with group 15 chlorides, ECl3 (E = P, Sb) to form the Lewis adducts BICAAC:ECl3 (E = P (1), Sb (2)) has been investigated in the present work. The BICAAC smoothly reacts with PPhCl2 to form [BICAAC:PPhCl2] which on in‐situ two electron reduction with 2 equivalents of KC8 afforded the phosphinidene complex, BICAAC=P‐Ph (3). Complete dechlorination of the BICAAC‐ECl3 adducts 1 and 2 with 3 equivalents of KC8 leads to three‐electron reduction … Show more
The synthesis and reactivity of an air and water stable Bicyclic (alkyl)(amino)carbene (BICAAC) stabilized phosphenium cation (1) is reported. Air and water stable phosphenium cation are rare in the literature. Compound 1 is obtained by reaction of BICAAC with Ph2PCl in THF followed by anion exchange with LiOTf. The reduction and oxidation of 1 yielded corresponding α‐radical phosphine species (2) and BICAAC stabilized phosphenium oxide (3) respectively. All compounds are well characterized by single crystal X‐ray diffraction studies. The Lewis acidity of compounds 1 and 3 are determined by conducting fluoride ion affinity experiments using UV‐Vis spectrophotometry and multinuclei NMR spectroscopy. Compounds 1 and 3 exhibited selective binding to fluoride anion but did not interact with other halides (Cl‐ and Br‐). Quantum chemical calculations were performed to understand the structure and nature of bonding interactions in these compounds, as well as to comprehend the specific bonding affinity to fluoride over other halide ions.
The synthesis and reactivity of an air and water stable Bicyclic (alkyl)(amino)carbene (BICAAC) stabilized phosphenium cation (1) is reported. Air and water stable phosphenium cation are rare in the literature. Compound 1 is obtained by reaction of BICAAC with Ph2PCl in THF followed by anion exchange with LiOTf. The reduction and oxidation of 1 yielded corresponding α‐radical phosphine species (2) and BICAAC stabilized phosphenium oxide (3) respectively. All compounds are well characterized by single crystal X‐ray diffraction studies. The Lewis acidity of compounds 1 and 3 are determined by conducting fluoride ion affinity experiments using UV‐Vis spectrophotometry and multinuclei NMR spectroscopy. Compounds 1 and 3 exhibited selective binding to fluoride anion but did not interact with other halides (Cl‐ and Br‐). Quantum chemical calculations were performed to understand the structure and nature of bonding interactions in these compounds, as well as to comprehend the specific bonding affinity to fluoride over other halide ions.
BICAAC (bicyclic (alkyl)(amino)carbene) as ambiphilic carbene has been utilized to prepare stable neutral tetrahydrodiborane [BICAAC→(H2)B‐B(H2)←BICAAC] and dihydrodiborene [BICAAC→(H)B=B(H)←BICAAC] compounds. The Lewis base stabilized dihydrodiborene is isoelectronic and isolobal to conventional olefins and therefore offers the possibility to explore the formation of π‐complexes with transition metals. Reaction of the diborene with coinage metal salts (CuCl, AgBr and CuI) leads to the formation of π‐diborene metal complexes via η2 side‐on coordination. These are first examples of dihydrodiborene coinage metal complexes. Interestingly, coordination of two CuCl units to the diborene has been observed for the first time with a considerable lengthening of >B=B< and B‐CBICAAC bonds manifesting the key role of the BICAAC combined with small steric requirements of hydride substituents in stabilizing these complexes. The energy decomposition analysis (EDA) calculations reveal the interaction between the diborene and Cu(I)/Ag(I) is mainly electrostatic in nature.
Herein, the synthesis and characterization of the bicyclic (alkyl)(amino)carbene (BICAAC) stabilized phosphinidenes (1–4) are reported. Compounds 1–3 were obtained by reacting with trihalophosphine [PX3, X = Cl (1), Br (2),...
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