Aldiminium and 1,2,3-triazolium dithiocarboxylate zwitterions derived from cyclic (alkyl)(amino) and mesoionic carbenes

• Nedra Touj,
• François Mazars,
• Guillermo Zaragoza and
• Lionel Delaude

Beilstein J. Org. Chem. 2023, 19, 1947–1956, doi:10.3762/bjoc.19.145

• applications [24][25][26][27][28]. N-Heterocyclic carbenes and their enetetramine dimers readily add to the central carbon atom of allenes and heteroallenes X=C=Y (X, Y = CR2, NR, O, S) to afford zwitterionic adducts [29]. In particular, their reaction with carbon disulfide affords stable azolium-2

• instantaneous formation of the desired zwitterionic adducts, as evidenced by the appearance of an intense orange-red color. The solvent was removed and the residues were brought back to air, washed with n-pentane, and dried under high vacuum to afford pseudo-cross-conjugated mesomeric betaines 4a–c in high

Efficient CO₂ capture by tertiary amine-functionalized ionic liquids through Li⁺-stabilized zwitterionic adduct formation

• Zhen-Zhen Yang and
• Liang-Nian He

Beilstein J. Org. Chem. 2014, 10, 1959–1966, doi:10.3762/bjoc.10.204

• through formation of zwitterionic adducts, combining synthetic strategies to ionic liquids (ILs) and coordination. The essence of our strategy is to make use of multidentate cation coordination between Li+ and an organic base. Also PEG-functionalized organic bases were employed to enhance the CO2

• (mol CO2 absorbed per mol of base) through the formation of zwitterionic adducts being stabilized by Li+. Keywords: carbon capture and sequestration; CO2 chemistry; coordination effect; ionic liquid; polyethylene glycol; zwitterionic adducts; Introduction Carbon capture and sequestration (CCS) from

• were reacted then with CO2 to form intramolecular zwitterionic adducts. Results and Discussion Taking PEG150MeTMG as a neutral ligand (Table 1), coordination effects of various lithium salts were investigated (Table S1, Supporting Information File 1). Only LiSO3CF3 and LiNTf2 formed complexes with

Cation affinity numbers of Lewis bases

• Christoph Lindner,
• Raman Tandon,
• Boris Maryasin,
• Evgeny Larionov and
• Hendrik Zipse

Beilstein J. Org. Chem. 2012, 8, 1406–1442, doi:10.3762/bjoc.8.163

• zwitterionic adduct as defined in equation 10 is exergonic, which is in remarkable contrast to the energetics calculated for all cationic electrophiles above. Zwitterionic adducts formed by pyridine 63 are somewhat more stable than those formed by triphenylphosphane (89). These energetics parallel results