{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T08:38:20Z","timestamp":1788856700470,"version":"build-2803163510"},"reference-count":100,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2026,6,30]],"date-time":"2026-06-30T00:00:00Z","timestamp":1782777600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,6,30]],"date-time":"2026-06-30T00:00:00Z","timestamp":1782777600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["ChemistryOpen"],"published-print":{"date-parts":[[2026,7]]},"abstract":"<jats:p>\n                    The syntheses and structural elucidations of 16 novel compounds, derived from methane(poly\u2010)sulfonic acids are presented. The anhydrous acids, that is, methanedisulfonic acid (MDSA\u2014(H\n                    <jats:sub>2<\/jats:sub>\n                    C(SO\n                    <jats:sub>3<\/jats:sub>\n                    H)\n                    <jats:sub>2<\/jats:sub>\n                    ,\n                    <jats:bold>1<\/jats:bold>\n                    ) and methanetrisulfonic acid (MTSA), the latter as two polymorphic structures (HC(SO\n                    <jats:sub>3<\/jats:sub>\n                    H)\n                    <jats:sub>3<\/jats:sub>\n                    \u2010I (\n                    <jats:italic>P<\/jats:italic>\n                    3\n                    <jats:italic>c<\/jats:italic>\n                    1,\n                    <jats:bold>2<\/jats:bold>\n                    ) and HC(SO\n                    <jats:sub>3<\/jats:sub>\n                    H)\n                    <jats:sub>3<\/jats:sub>\n                    \u2010II (\n                    <jats:italic>P<\/jats:italic>\n                    2\n                    <jats:sub>1<\/jats:sub>\n                    \/\n                    <jats:italic>n<\/jats:italic>\n                    ,\n                    <jats:bold>3<\/jats:bold>\n                    )) have been crystallized and structurally elucidated. Methanedisulfonic acid was subsequently used to prepare four group I methanedisulfonates (AM\n                    <jats:sub>2<\/jats:sub>\n                    [(H\n                    <jats:sub>2<\/jats:sub>\n                    C(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>2<\/jats:sub>\n                    ], AM\u2009=\u2009Li (\n                    <jats:bold>6)<\/jats:bold>\n                    , K (\n                    <jats:bold>7<\/jats:bold>\n                    )\u00b7H\n                    <jats:sub>2<\/jats:sub>\n                    O, Rb (\n                    <jats:bold>8<\/jats:bold>\n                    ) and Cs (\n                    <jats:bold>10<\/jats:bold>\n                    )) as well as the strontium dihydrate Sr[H\n                    <jats:sub>2<\/jats:sub>\n                    C(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>2<\/jats:sub>\n                    ](H\n                    <jats:sub>2<\/jats:sub>\n                    O)\n                    <jats:sub>2<\/jats:sub>\n                    (\n                    <jats:bold>9<\/jats:bold>\n                    ) and the ternary salt BaK\n                    <jats:sub>2<\/jats:sub>\n                    [(H\n                    <jats:sub>2<\/jats:sub>\n                    C(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>2<\/jats:sub>\n                    ]\n                    <jats:sub>2<\/jats:sub>\n                    (\n                    <jats:bold>11<\/jats:bold>\n                    ). The known trisulfonate K\n                    <jats:sub>3<\/jats:sub>\n                    [HC(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>3<\/jats:sub>\n                    ](H\n                    <jats:sub>2<\/jats:sub>\n                    O) was used for the preparation of the oxonium salt [H\n                    <jats:sub>3<\/jats:sub>\n                    O]\n                    <jats:sub>3<\/jats:sub>\n                    [HC(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>3<\/jats:sub>\n                    ] (\n                    <jats:bold>4<\/jats:bold>\n                    ), which was isolated as a new polymorph (\n                    <jats:italic>R<\/jats:italic>\n                    3\n                    <jats:italic>c<\/jats:italic>\n                    ). Subsequent neutralization led to isolation of the compounds AM\n                    <jats:sub>3<\/jats:sub>\n                    [HC(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>3<\/jats:sub>\n                    ] (AM\u2009=\u2009Li (\n                    <jats:bold>12<\/jats:bold>\n                    )\u00b7(H\n                    <jats:sub>2<\/jats:sub>\n                    O)\n                    <jats:sub>4<\/jats:sub>\n                    , K (\n                    <jats:bold>13<\/jats:bold>\n                    ), Rb (\n                    <jats:bold>14<\/jats:bold>\n                    )\u00b7H\n                    <jats:sub>2<\/jats:sub>\n                    O, as well as the two ternary salts Rb\n                    <jats:sub>3<\/jats:sub>\n                    Ag\n                    <jats:sub>3<\/jats:sub>\n                    [HC(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>3<\/jats:sub>\n                    ]\n                    <jats:sub>2<\/jats:sub>\n                    (\n                    <jats:bold>15<\/jats:bold>\n                    ) and Rb\n                    <jats:sub>5<\/jats:sub>\n                    Ag[HC(SO\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>3<\/jats:sub>\n                    ]\n                    <jats:sub>2<\/jats:sub>\n                    (H\n                    <jats:sub>2<\/jats:sub>\n                    O)\n                    <jats:sub>2<\/jats:sub>\n                    (\n                    <jats:bold>16<\/jats:bold>\n                    ). For a structural comparison between a mono\u2010, di\u2010, and trisulfonate, we also prepared the still elusive rubidium methanesulfonate, which crystallizes as the hydrate Rb[H\n                    <jats:sub>3<\/jats:sub>\n                    C(SO\n                    <jats:sub>3<\/jats:sub>\n                    )](H\n                    <jats:sub>2<\/jats:sub>\n                    O) (\n                    <jats:bold>5<\/jats:bold>\n                    ). Different synthetic approaches, as well as an in\u2010depth structural analysis of all compounds, are presented. Furthermore, compound\n                    <jats:bold>8<\/jats:bold>\n                    and the oxonium salt of compound\n                    <jats:bold>1<\/jats:bold>\n                    were investigated concerning their thermal decomposition.\n                  <\/jats:p>","DOI":"10.1002\/open.70247","type":"journal-article","created":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T05:33:23Z","timestamp":1782884003000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["The Versatile Structural World of Methanedi\u2010 and Trisulfonic Acid and Their Salts"],"prefix":"10.1002","volume":"15","author":[{"ORCID":"https:\/\/orcid.org\/0009-0008-7399-1542","authenticated-orcid":false,"given":"Katrin","family":"Eppers","sequence":"first","affiliation":[{"name":"Institute of Inorganic and Materials Chemistry University of Cologne  Cologne 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