"1,2-Dithiete"@en . . . "Dithiacyclobutene"@en . "Ditiet \u2013 organiczny zwi\u0105zek chemiczny nale\u017C\u0105cy do nienasyconych zwi\u0105zk\u00F3w heterocyklicznych siarki. Ditiet zbudowany jest z pier\u015Bcienia, w sk\u0142ad kt\u00F3rego wchodz\u0105 dwa atomy w\u0119gla i dwa atomy siarki, b\u0119d\u0105ce heteroatomami. Ditiet mo\u017Cna traktowa\u0107 jako disiarkowy analog dioksetu."@pl . . . . . "100"^^ . . "Dithiete"@en . . . . . . . . . "12"^^ . . "6729"^^ . "12"^^ . . "\u30B8\u30C1\u30A8\u30C8(Dithiete)\u306F\u30012\u3064\u306E\u96A3\u63A5\u786B\u9EC4\u539F\u5B50\u30012\u3064\u306E[[SP2\u6DF7\u6210|\u6DF7\u6210\u8ECC\u9053]]\u70AD\u7D20\u4E2D\u5FC3\u3092\u542B\u3080\u4E0D\u98FD\u548C\u8907\u7D20\u74B0\u5F0F\u5316\u5408\u7269\u3067\u3042\u308B\u3002\u304C\u3042\u308A\u3001\u82B3\u9999\u6027\u3092\u6301\u3064\u3002\u5C11\u91CF\u304C\u5358\u96E2\u3055\u308C\u3066\u3044\u308B\u3002 \u975E\u7F6E\u63DB1,2-\u30B8\u30C1\u30A8\u30C8\u306F\u71B1\u5206\u89E3\u53CD\u5FDC\u3067\u751F\u6210\u3057\u3001\u30DE\u30A4\u30AF\u30ED\u6CE2\u5206\u5149\u6CD5\u3001\u7D2B\u5916\u5149\u96FB\u5B50\u5206\u5149\u6CD5\u3001\u304A\u3088\u3073\u4F4E\u6E29\u30DE\u30C8\u30EA\u30C3\u30AF\u30B9\u3067\u306E\u8D64\u5916\u5206\u5149\u6CD5\u306B\u3088\u308B\u5206\u6790\u3092\u53D7\u3051\u305F\u3002\u958B\u74B0\u7570\u6027\u4F53(HC(S)C(S)H)\u306F\u3001\u3088\u308A\u4E0D\u5B89\u5B9A\u3067\u3042\u308B\u3002 \u306F\u3001\u306E\u4F4E\u6E29\u5149\u5206\u89E3\u306B\u3088\u308A\u751F\u6210\u3059\u308B\u3002\u91CF\u5B50\u5316\u5B66\u8A08\u7B97\u3067\u306F\u3001\u3092\u6301\u3064\u5927\u304D\u306A\u57FA\u5E95\u95A2\u6570\u304C\u4F7F\u7528\u3055\u308C\u308B\u5834\u5408\u306B\u306E\u307F\u3001\u89B3\u6E2C\u3055\u308C\u308B1,2-\u30B8\u30C1\u30A8\u30C8\u306E\u5B89\u5B9A\u6027\u304C\u518D\u73FE\u3055\u308C\u308B\u3002"@ja . . . . "1,2-Dithiacyclobut-3-ene"@en . . "Dithiacyclobutene"@en . . . . . . . . . . . . . . . . . "Kekul\u00E9, skeletal formula of dithiete with all explicit hydrogens added"@en . . . . . "14290918"^^ . . . . . "Ditiet \u2013 organiczny zwi\u0105zek chemiczny nale\u017C\u0105cy do nienasyconych zwi\u0105zk\u00F3w heterocyklicznych siarki. Ditiet zbudowany jest z pier\u015Bcienia, w sk\u0142ad kt\u00F3rego wchodz\u0105 dwa atomy w\u0119gla i dwa atomy siarki, b\u0119d\u0105ce heteroatomami. Ditiet mo\u017Cna traktowa\u0107 jako disiarkowy analog dioksetu."@pl . "Dithiete.svg"@en . . . "1,2-Dithia[4]annulene"@en . . . "Dithiete is an unsaturated heterocyclic compound that contains two adjacent sulfur atoms and two sp2-hybridized carbon centers. Derivatives are known collectively as dithietes or 1,2-dithietes. With 6 \u03C0 electrons, 1,2-dithietes are examples of aromatic organosulfur compounds. A few 1,2-dithietes have been isolated. Unsubstituted 1,2-dithiete has been generated in thermolytic reactions and was characterized by microwave spectroscopy, ultraviolet photoelectron spectroscopy and infrared spectroscopy in a low temperature matrix. The open ring isomer, dithioglyoxal, HC(S)C(S)H, is less stable than the 1,2-dithiete. The dithione can be prepared (as trans-dithioglyoxal) by low temperature photolysis of 1,3-dithiol-2-one. Quantum chemical calculations reproduce the observed greater stability of 1,2-dithiete only if large basis-sets with polarization functions are used."@en . . . . . . "Dithiete"@en . . "\u30B8\u30C1\u30A8\u30C8"@ja . . . . . "Dithiete"@en . . . . . "1085761478"^^ . . . "12"^^ . "Dithiete is an unsaturated heterocyclic compound that contains two adjacent sulfur atoms and two sp2-hybridized carbon centers. Derivatives are known collectively as dithietes or 1,2-dithietes. With 6 \u03C0 electrons, 1,2-dithietes are examples of aromatic organosulfur compounds. A few 1,2-dithietes have been isolated. The dithione can be prepared (as trans-dithioglyoxal) by low temperature photolysis of 1,3-dithiol-2-one. Quantum chemical calculations reproduce the observed greater stability of 1,2-dithiete only if large basis-sets with polarization functions are used."@en . "\u30B8\u30C1\u30A8\u30C8(Dithiete)\u306F\u30012\u3064\u306E\u96A3\u63A5\u786B\u9EC4\u539F\u5B50\u30012\u3064\u306E[[SP2\u6DF7\u6210|\u6DF7\u6210\u8ECC\u9053]]\u70AD\u7D20\u4E2D\u5FC3\u3092\u542B\u3080\u4E0D\u98FD\u548C\u8907\u7D20\u74B0\u5F0F\u5316\u5408\u7269\u3067\u3042\u308B\u3002\u304C\u3042\u308A\u3001\u82B3\u9999\u6027\u3092\u6301\u3064\u3002\u5C11\u91CF\u304C\u5358\u96E2\u3055\u308C\u3066\u3044\u308B\u3002 \u975E\u7F6E\u63DB1,2-\u30B8\u30C1\u30A8\u30C8\u306F\u71B1\u5206\u89E3\u53CD\u5FDC\u3067\u751F\u6210\u3057\u3001\u30DE\u30A4\u30AF\u30ED\u6CE2\u5206\u5149\u6CD5\u3001\u7D2B\u5916\u5149\u96FB\u5B50\u5206\u5149\u6CD5\u3001\u304A\u3088\u3073\u4F4E\u6E29\u30DE\u30C8\u30EA\u30C3\u30AF\u30B9\u3067\u306E\u8D64\u5916\u5206\u5149\u6CD5\u306B\u3088\u308B\u5206\u6790\u3092\u53D7\u3051\u305F\u3002\u958B\u74B0\u7570\u6027\u4F53(HC(S)C(S)H)\u306F\u3001\u3088\u308A\u4E0D\u5B89\u5B9A\u3067\u3042\u308B\u3002 \u306F\u3001\u306E\u4F4E\u6E29\u5149\u5206\u89E3\u306B\u3088\u308A\u751F\u6210\u3059\u308B\u3002\u91CF\u5B50\u5316\u5B66\u8A08\u7B97\u3067\u306F\u3001\u3092\u6301\u3064\u5927\u304D\u306A\u57FA\u5E95\u95A2\u6570\u304C\u4F7F\u7528\u3055\u308C\u308B\u5834\u5408\u306B\u306E\u307F\u3001\u89B3\u6E2C\u3055\u308C\u308B1,2-\u30B8\u30C1\u30A8\u30C8\u306E\u5B89\u5B9A\u6027\u304C\u518D\u73FE\u3055\u308C\u308B\u3002"@ja . . . "Ditiet"@pl . . . . . .