Borenes and boranes: Silylaminoiminoborenes, such as depicted, were isolated after treatment of halogen triels with silylaminofluoroboranes. In addition, novel aryl- and silyl-substituted diaminofluoroboranes were also prepared in order to substantiate this reaction route.Reactions between the halogen triels AlClMe(2), AlBr(3), GaCl(3) and the silylaminofluoroboranes (Me(3)Si)(2)NB(F)NRSiMe(3) (R=SiMe(3), CMe(3)) afforded the silylaminoiminoborenes, which were isolated as the triel adducts, such as Me(3)Si(Cl(3)Ga)NBNRSiMe(3) (6). In order to extent this reaction path to other fluoroboranes, novel aryl- and silyl-substituted diaminofluoroboranes were synthesised. Because almost no open-chain diaminofluoroboranes had been structurally characterised previously, corresponding fluoroboranes containing no silyl groups were crystallised for purposes of comparison. In complex reactions with the arylsilylaminofluoroboranes [(2,6-(iPr)(2)C(6)H(3))(Me(3)Si)NB(F)NR(2), R=iPr, iBu], amine adducts of borenium salts such as [(iPr)(2)NH-->B(Bu)NH-2,6-(iPr)(2)C(6)H(3)](+)AlCl(4) (-) (13) were obtained.
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http://dx.doi.org/10.1002/chem.200802669 | DOI Listing |
J Phys Chem A
June 2024
Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, Gdańsk 80-308, Poland.
The abundance of XIII group element compounds in science and industry together with their electron-deficient character gives rise to their influence on properties of the systems they interact with. This paper is an attempt to assess the strength, nature, and effect of formation of a triel bond on acidity. A wide set of Brønsted acids among others comprising hydrocarbons, halogen hydrides, and amines bonded with B, Al, and Ga trifluorides forming HX/TF was selected for the research.
View Article and Find Full Text PDFChemphyschem
March 2023
Laboratory of Theoretical and Computational Chemistry and School of Chemistry and Chemical Engineering, Yantai University, Yantai, 264005, China.
The novel triel bonds of BX (X=H, F, Cl, Br, and I) and C H B as electron acceptors and AuR (R=Cl and CH ) as an electron donor were explored. The triel bond is a primary driving force for most complexes, while the contribution from a halogen-chlorine interaction in BX -AuCl (X=Cl, Br, and I) and an iodine-Au interaction in BI -Au(CH ) is also very important. Interestingly, the positively charged Au atom of AuCl can attractively bind with the holes of BX and C H B.
View Article and Find Full Text PDFMolecules
September 2022
The Laboratory of Theoretical and Computational Chemistry, School of Chemistry and Chemical Engineering, Yantai University, Yantai 264005, China.
Malondialdehyde (MDA) engages in a triel bond (TrB) with TrX (Tr = B and Al; X = H, F, Cl, and Br) in three modes, in which the hydroxyl O, carbonyl O, and central carbon atoms of MDA act as the electron donors, respectively. A H···X secondary interaction coexists with the TrB in the former two types of complexes. The carbonyl O forms a stronger TrB than the hydroxyl O, and both of them are better electron donors than the central carbon atom.
View Article and Find Full Text PDFChem Soc Rev
June 2022
School of Chemical Sciences, National Institute of Science Education and Research (NISER), PO- Bhimpur-Padanpur, Via-Jatni, District- Khurda, PIN - 752050, Bhubaneswar, India.
Understanding the noncovalent interactions (NCIs) among the residues of proteins and nucleic acids, and between drugs and proteins/nucleic acids, , has extraordinary relevance in biomolecular structure and function. It helps in interpreting the dynamics of complex biological systems and enzymatic activity, which is esential for new drug design and efficient drug delivery. NCIs like hydrogen bonding (H-bonding) and π-stacking have been researchers' delight for a long time.
View Article and Find Full Text PDFPhys Chem Chem Phys
November 2021
Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84322-0300, USA.
The ability of two anions to interact with one another is tested in the context of pairs of TrX homodimers, where Tr represents any of the triel atoms B, Al, Ga, In, or Tl, and X refers to a halogen substituent F, Cl, or Br. None of these pairs engage in a stable complex in the gas phase, but the situation reverses in water where the two monomers are held together by Tr⋯X triel bonds, complemented by stabilizing interactions between X atoms. Some of these bonds are quite strong, notably those involving TrF, with interaction energies surpassing 30 kcal mol.
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