It is evidenced through vibrational spectroscopy that a heterodimer or "Quadac" is formed when an excess of base (LHMDS, LDA, or n-BuLi) is added to PhCH(2)CN in THF, THF-hexane, or THF-toluene solution. The amount of heterodimer increases with the pK(H)(a) of the lithiated base. A dianionic species may be formed through decomposition of this heterodimer if the pK(H)(a) of the base is sufficiently high, as in the case of n-BuLi. With LDA, only a very small amount of dianion is observed, and with LHMDS, no dianion is detected. The predominant dianionic species observed are the linear and bridged separated ion pairs of the dilithiated dianion. The presence of the amine in the medium is of paramount importance. The PhCHCNLi monomer-dimer equilibrium is entropy driven toward the dimer solvated by the amine.
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http://dx.doi.org/10.1021/jo020492t | DOI Listing |
ACS Polym Au
December 2024
Forschungszentrum Jülich GmbH, Helmholtz Institute Erlangen-Nürnberg for Renewable Energy (IET-2), Cauerstraße 1, 91058 Erlangen, Germany.
Polyethersulfone (PSU) as a commercially available polymer offers many different opportunities for functionalization for diverse fields of application, for example, electrophilic substitutions like sulfonation and bromination or nucleophilic reactions such as lithiation. This study presents three different polysulfone derivatives, first functionalized by a lithiation reaction, followed by a reaction with carbonyl compounds containing pentafluorophenyl groups. In the last step, the pentafluorophenyl moieties of the modified PSU were sulfonated by thiolation and subsequent oxidation to sulfonic acid groups.
View Article and Find Full Text PDFAnal Chim Acta
August 2024
Koichi Tanaka Mass Spectrometry Research Laboratory, Shimadzu Corporation, Kyoto, 604-8511, Japan.
ACS Appl Mater Interfaces
July 2024
College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, P. R. China.
Under the background of "carbon neutral", lithium-ion batteries (LIB) have been widely used in portable electronic devices and large-scale energy storage systems, but the current commercial electrolyte is mainly liquid organic compounds, which have serious safety risks. In this paper, a bilayer heterogeneous composite solid-state electrolyte (PLPE) was constructed with the 3D LiX zeolite nanofiber (LiX-NF) layer and in-situ interfacial layer, which greatly extends the life span of lithium metal batteries (LMB). LiX-NF not only offers a continuous fast path for Li, but also zeolite's Lewis acid-base interaction can immobilize large anions, which significantly improves the electrochemical performance of the electrolyte.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
April 2024
Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Iran.
In this study, the effect of different numbers of Li interacting with various sites of DNA base pairs (adenine-thymine (AT) and cytosine-guanine (GC)) on the base pair structures, the strength of hydrogen bonding between the bases, and spectroscopic properties (IR and absorption spectra) of the base pairs was investigated. Two quantum computational analyses, the natural bonding orbitals (NBO) and the quantum theory of atoms in molecules (QTAIM), were used to follow the change in the strength of hydrogen bonds between the bases in each pair. The type of base pair's site interacting with Li showed different effects on the change in the strength of the hydrogen bonds between the bases.
View Article and Find Full Text PDFJ Org Chem
January 2024
A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St., Irkutsk 664033, Russian Federation.
Self-assembly of 4,4'-linked dipyrromethanes from 2-(vinyloxy)ethyl isothiocyanate, tertiary propargylamines, and alkylating agents has been discovered. The plausible reaction mechanism, the major stages of which have been confirmed experimentally, includes (1) the lithiation of propargylamine (with -BuLi); (2) the formation of lithium -[2-(vinyloxy)ethyl]but-2-ynimidothioate (product of the addition of monolithiated propargylamine to isothiocyanate); (3) isomerization of the latter in the corresponding allenylimidothioate (under the action of the -BuOK/-BuOH system); (4) low-temperature (<15 °C) intramolecular cyclization of the latter into potassium -(5-amino-2-thienyl)--[2-(vinyloxy)ethyl]amide; (5) the base-induced cleavage of the C-O bond of the -[2-(vinyloxy)ethyl] group and removal of vinyloxide-anion leading to acetaldehyde; (6) interaction of acetaldehyde with two molecules of -(5-amino-2-thienyl)--[2-(vinyloxy)ethyl]amide-anion resulting in dithienomethane N-anionic intermediate; (7) recyclization of the latter into dipyrromethane S-anionic intermediate. Final S-alkylation affords synthetically challenging 4,4'-dipyrromethanes in a yield of 22-51%.
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