{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,23]],"date-time":"2026-08-23T14:42:30Z","timestamp":1787496150892,"version":"build-2736575974"},"reference-count":89,"publisher":"Wiley","issue":"50","license":[{"start":{"date-parts":[[2014,10,15]],"date-time":"2014-10-15T00:00:00Z","timestamp":1413331200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Chemistry A European J"],"published-print":{"date-parts":[[2014,12,8]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    To gain more insight into the reactivity of intermetalloid clusters, the reactivity of the Zintl phase K\n                    <jats:sub>12<\/jats:sub>\n                    Sn\n                    <jats:sub>17<\/jats:sub>\n                    , which contains [Sn\n                    <jats:sub>4<\/jats:sub>\n                    ]\n                    <jats:sup>4\u2212<\/jats:sup>\n                    and [Sn\n                    <jats:sub>9<\/jats:sub>\n                    ]\n                    <jats:sup>4\u2212<\/jats:sup>\n                    cluster anions, was investigated. The reaction of K\n                    <jats:sub>12<\/jats:sub>\n                    Sn\n                    <jats:sub>17<\/jats:sub>\n                    with gold(I) phosphine chloride yielded K\n                    <jats:sub>7<\/jats:sub>\n                    [(\u03b7\n                    <jats:sup>2<\/jats:sup>\n                    \u2010Sn\n                    <jats:sub>4<\/jats:sub>\n                    )Au(\u03b7\n                    <jats:sup>2<\/jats:sup>\n                    \u2010Sn\n                    <jats:sub>4<\/jats:sub>\n                    )](NH\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>16<\/jats:sub>\n                    (\n                    <jats:bold>1<\/jats:bold>\n                    ) and K\n                    <jats:sub>17<\/jats:sub>\n                    [(\u03b7\n                    <jats:sup>2<\/jats:sup>\n                    \u2010Sn\n                    <jats:sub>4<\/jats:sub>\n                    )Au(\u03b7\n                    <jats:sup>2<\/jats:sup>\n                    \u2010Sn\n                    <jats:sub>4<\/jats:sub>\n                    )]\n                    <jats:sub>2<\/jats:sub>\n                    (NH\n                    <jats:sub>2<\/jats:sub>\n                    )\n                    <jats:sub>3<\/jats:sub>\n                    (NH\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>52<\/jats:sub>\n                    (\n                    <jats:bold>2<\/jats:bold>\n                    ), which both contain the anion [(Sn\n                    <jats:sub>4<\/jats:sub>\n                    )Au(Sn\n                    <jats:sub>4<\/jats:sub>\n                    )]\n                    <jats:sup>7\u2212<\/jats:sup>\n                    (\n                    <jats:bold>1\u2009a<\/jats:bold>\n                    ) that consists of two [Sn\n                    <jats:sub>4<\/jats:sub>\n                    ]\n                    <jats:sup>4\u2212<\/jats:sup>\n                    tetrahedra linked through a central gold atom. Anion\n                    <jats:bold>1\u2009a<\/jats:bold>\n                    represents the first binary Au\uf8ffSn polyanion. From this reaction, the solvate structure [K([2.2.2]crypt)]\n                    <jats:sub>3<\/jats:sub>\n                    K[Sn\n                    <jats:sub>9<\/jats:sub>\n                    ](NH\n                    <jats:sub>3<\/jats:sub>\n                    )\n                    <jats:sub>18<\/jats:sub>\n                    (\n                    <jats:bold>3<\/jats:bold>\n                    ; [2.2.2]crypt=4,7,13,16,21,24\u2010hexaoxa\u20101,10\u2010diazabicyclo[8.8.8]hexacosane) was also obtained. In the analogous reaction of mesitylcopper with K\n                    <jats:sub>12<\/jats:sub>\n                    Sn\n                    <jats:sub>17<\/jats:sub>\n                    in the presence of [18]crown\u20106 in liquid ammonia, crystals of the composition [K([18]crown\u20106)]\n                    <jats:sub>2<\/jats:sub>\n                    [K([18]crown\u20106)(MesH)(NH\n                    <jats:sub>3<\/jats:sub>\n                    )][Cu@Sn\n                    <jats:sub>9<\/jats:sub>\n                    ](thf) (\n                    <jats:bold>4<\/jats:bold>\n                    ) were isolated ([18]crown\u20106=1,4,7,10,13,16\u2010hexaoxacyclooctadiene, MesH=mesitylene, thf=tetrahydrofuran) and featured a [Cu@Sn\n                    <jats:sub>9<\/jats:sub>\n                    ]\n                    <jats:sup>3\u2212<\/jats:sup>\n                    cluster. A similar reaction with [2.2.2]crypt as a sequestering agent led to the formation of crystals of [K[2.2.2]crypt][MesCuMes] (\n                    <jats:bold>5<\/jats:bold>\n                    ). The cocrystallization of mesitylene in\n                    <jats:bold>4<\/jats:bold>\n                    and the presence of [MesCuMes]\n                    <jats:sup>\u2212<\/jats:sup>\n                    (\n                    <jats:bold>5\u2009a<\/jats:bold>\n                    ) in\n                    <jats:bold>5<\/jats:bold>\n                    provides strong evidence that the migration of a bare Cu atom into an Sn\n                    <jats:sub>9<\/jats:sub>\n                    anion takes place through the release of a Mes\n                    <jats:sup>\u2212<\/jats:sup>\n                    anion from mesitylcopper, which either migrates to another mesitylcopper to form\n                    <jats:bold>5\u2009a<\/jats:bold>\n                    or is subsequently protonated to give MesH.\n                  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