Sulfite esters as products of the interaction in sulfur dioxide – alkanol – tris(hydroxymethyl)aminomethane systems

References

• Günther A, König T, Habicher WD, et al. Antioxidant action of organic sulfites – II. Esters of sulfurous acid as primary antioxidants. Polym Degrad Stab. 1998;60(2–3):385–391. doi:10.1016/S0141-3910(97)00098-0
   Web of Science ®Google Scholar
• Günther A, König T, Habicher WD, et al. Antioxidant action of organic sulphites – I. Esters of sulphurous acid as secondary antioxidants. Polym Degrad Stab. 1997;55(2):209–216. doi:10.1016/S0141-3910(96)00150-4
   Web of Science ®Google Scholar
• Günther A, König T, Habicher WD, et al. Antioxidant action of organic sulphites III. Antioxidative effect of esters of sulphurous acid in hydrocarbons and polypropylene. Polym Degrad Stab. 1999;64(1):115–126. doi:10.1016/S0141-3910(98)00184-0
   Web of Science ®Google Scholar
• Grünke S, Wünsch G. Kinetics and stoichiometry in the Karl Fischer solution. Fresenius J Anal Chem. 2000;368:139–147. doi:10.1007/s002160000444
   PubMedGoogle Scholar
• Varghese TS, Mathew TB. Bioefficacy and safety evaluation of newer insecticides and acaricides against chilli thrips and mites. J Tropical Agric. 2013;51(1):111–115.
   Google Scholar
• Evans TD, Howe TM, inventor; Biocidal formulation. World Intellectual Property Organization patent WO2008040987. 2008 Apr 10.
   Google Scholar
• Ignatiev N, Welz-Biermann U, Kucheryna A, et al., inventor; Merck Patent GmbH, assignee. Process for the preparation of onium alkyl sulfites. German patent DE102005032837. 2007 Feb 08.
   Google Scholar
• Bao R, Feng Y, Deng D, et al. Sulfinic acids in organic synthesis: a review of recent studies. Asian J Org Chem. 2021;10(8):1884–1896. doi:10.1002/ajoc.202100331
   Web of Science ®Google Scholar
• Baek GH, Jang HT, Cha WS. Absorption characteristic of carbon dioxide in ionic liquids based sulfite anion in the pre-combustion condition. J Korea Acad-Ind Cooperation Soc. 2021;22(3):763–769.
   Google Scholar
• Akashi H, Hara T, Ogawa K, et al., inventor; Sony Corp, assignee. Battery. Japan patent JP2006302757A. 2006 Nov 02.
   Google Scholar
• Ping P, Wang QS, Sun JH, et al. Effect of sulfites on the performance of LiBOB/γ-butyrolactone electrolytes. J Power Sources. 2011;196(2):776–783. doi:10.1016/j.jpowsour.2010.07.064
   Web of Science ®Google Scholar
• Mao L, Li B, Cui X, et al. Electrochemical performance of electrolytes based upon lithium bis(oxalate)borate and sulfolane/alkyl sulfite mixtures for high temperature lithium-ion batteries. Electrochim Acta. 2012;79:197–201. doi:10.1016/j.electacta.2012.06.102
   Web of Science ®Google Scholar
• McCormack WB, Lawes BC. Sulfuric and sulfurous esters. In: Kirk-Othmer encyclopaedia of chemical technology. John Wiley and Sons; 2001. doi:10.1002/0471238961.1921120613030315.a01
   Google Scholar
• Heldebrant DJ, Yonker CR, Jessop PG, et al. Reversible uptake of COS, CS2, and SO2: ionic liquids with O-alkylxanthate, O-alkylthiocarbonyl, and O-alkylsulfite anions. Chem Eur J. 2009;15(31):7619–7627. doi:10.1002/chem.200802602
   PubMed Web of Science ®Google Scholar
• Heldebrant DJ, Koech PK, Yonker CR. A reversible zwitterionic SO2-binding organic liquid. Energy Env Sci. 2010;3(1):111–113. doi:10.1039/b916550a
   Web of Science ®Google Scholar
• Borba A, Gómez-Zavaglia A, Simões PNNL, et al. Matrix isolation FTIR spectroscopic and theoretical study of dimethyl sulfite. J Phys Chem A. 2005;109(16):3578–3586. doi:10.1021/jp050020t
   PubMed Web of Science ®Google Scholar
• Khoma RE, Gelmboldt VO, Shishkin OV, et al. Synthesis, crystal structure, vibrational spectra, and thermochemical transformations of tris(hydroxymethyl)aminomethane. Russ J Inorg Chem. 2014;59(1):1–6. doi:10.1134/S0036023614010069
   Google Scholar
• Kumar SS, Nangia A. A solubility comparison of neutral and Zwitterionic polymorphs. Cryst Growth Des. 2014;14(4):1865–1881. doi:10.1021/cg5000205
   Web of Science ®Google Scholar
• Minkov VS, Goryainov SV, Boldyreva EV, et al. Raman study of pressure-induced phase transitions in crystals of orthorhombic and monoclinic polymorphs of L-cysteine: dynamics of the side chain. J Raman Spectrosc. 2010;41(12):1748–1758. doi:10.1002/jrs.2624
   Web of Science ®Google Scholar
• Khoma RE, Gelmboldt VO, Ennan AA, et al. Synthesis and spectral characteristics of tris(hydroxymethyl)methylammonium sulfite. Voprosy Khimii i Khimicheskoi Tekhnologii. 2020;(4):172–176. doi:10.32434/0321-4095-2020-131-4-172-176
   Google Scholar
• Gordon AJ, Ford RA. The chemist’s companion: a handbook of practical data, techniques, and references. New York: Wiley; 1973; 560 p.
   Google Scholar
• Sheldrick GM. SHELXT - integrated space-group and crystal-structure determination. Acta Cryst. 2015;A71(1):3–8. doi:10.1107/s2053273314026370
   Google Scholar
• Sheldrick GM. Crystal structure refinement with SHELXL. Acta Cryst. 2015;C71(1):3–8. doi:10.1107/s2053229614024218
   Google Scholar
• Farrugia LJ. WinGXsuite for small-molecule single-crystal crystallography. J Appl Crystallogr. 1999;32(4):837–838. doi:10.1107/s0021889899006020
   Google Scholar
• Rodriguez-Carvajal J, Roisnel T. Fullprof.98 and WinPLOTR: new Windows 95/NT applications for diffraction. Commission for powder diffraction. Int Union Crystallogr. 1998 May-Aug;20:35–36.
   Google Scholar