. . . . . . "El octacarbonilo de dicobalto es el compuesto inorg\u00E1nico Co2(CO)8. Este carbonilo met\u00E1lico es un reactivo y catalizador usado en qu\u00EDmica organomet\u00E1lica y s\u00EDntesis org\u00E1nica.\u200B Se utiliza como catalizador para la reacci\u00F3n de hidroformilaci\u00F3n (conversi\u00F3n de alquenos en aldeh\u00EDdos).\u200B"@es . . . . . "Dicobalt octacarbonyl is an organocobalt compound with composition Co2(CO)8. This metal carbonyl is used as a reagent and catalyst in organometallic chemistry and organic synthesis, and is central to much known organocobalt chemistry. It is the parent member of a family of hydroformylation catalysts. Each molecule consists of two cobalt atoms bound to eight carbon monoxide ligands, although multiple structural isomers are known. Some of the carbonyl ligands are labile."@en . "172800.0"^^ . . . . . . . . "Dicobaltoctacarbonyl ist ein zweikerniger Komplex, bei dem zwei Cobaltkerne von acht Carbonylliganden umgeben sind."@de . . "Dicobalt-octacarbonyl-D3d-non-bridged-from-C60-xtal-2009-3D-balls.png"@en . . "Dicobalt octacarbonyl"@en . . . . . . . . "Dikobaltoctacarbonyl is het anorganische kobaltverbinding met als formule Co2(CO)8. De stof komt voor als oranje kristallen, die onoplosbaar zijn in water. De stof is pyrofoor."@nl . "\u062B\u0645\u0627\u0646\u064A \u0643\u0631\u0628\u0648\u0646\u064A\u0644 \u062B\u0646\u0627\u0626\u064A \u0627\u0644\u0643\u0648\u0628\u0627\u0644\u062A"@ar . "Dicobalt-octacarbonyl-D2d-non-bridged-3D-balls.png"@en . . . . . . "changed"@en . . "\u062B\u0645\u0627\u0646\u064A \u0643\u0631\u0628\u0648\u0646\u064A\u0644 \u062B\u0646\u0627\u0626\u064A \u0627\u0644\u0643\u0648\u0628\u0627\u0644\u062A \u0623\u0648 \u062B\u0645\u0627\u0646\u064A \u0643\u0631\u0628\u0648\u0646\u064A\u0644 \u0627\u0644\u0643\u0648\u0628\u0627\u0644\u062A \u0645\u0639\u0642\u062F \u0643\u0631\u0628\u0648\u0646\u064A\u0644 \u0644\u0647 \u0627\u0644\u0635\u064A\u063A\u0629 Co2(CO)8 \u060C \u0648\u064A\u0643\u0648\u0646 \u0639\u0644\u0649 \u0634\u0643\u0644 \u0628\u0644\u0648\u0631\u0627\u062A \u062D\u0645\u0631\u0627\u0621 \u0628\u0631\u062A\u0642\u0627\u0644\u064A\u0629."@ar . "Cobalt carbonyl , di-mu-Carbonylhexacarbonyldicobalt, Cobalt octacarbonyl, Cobalt tetracarbonyl dimer, Dicobalt carbonyl, Octacarbonyldicobalt"@en . . . . "Oktakarbonyl dikobaltu je organokovov\u00E1 slou\u010Denina se vzorcem Co2(CO)8. Pou\u017E\u00EDv\u00E1 se jako reagent a katalyz\u00E1tor v organokovov\u00E9 chemii a organick\u00E9 synt\u00E9ze. Ka\u017Ed\u00E1 molekula sest\u00E1v\u00E1 ze dvou atom\u016F kobaltu, kter\u00E9 jsou v\u00E1zan\u00E9 k osmi karbonylov\u00FDm ligand\u016Fm, d\u00EDky tomu je zn\u00E1mo v\u00EDce strukturn\u00EDch izomer\u016F. N\u011Bkter\u00E9 karbonylov\u00E9 ligandy jsou velmi labiln\u00ED. Slou\u010Denina ochotn\u011B reaguje s alkyny a proto se n\u011Bkdy vyu\u017E\u00EDv\u00E1 jako chr\u00E1n\u00EDc\u00ED skupina."@cs . . . . "\u516B\u7FB0\u57FA\u4E8C\u94B4\u662F\u4E00\u79CD\u65E0\u673A\u5316\u5408\u7269\uFF0C\u5316\u5B66\u5F0F\u4E3ACo2(CO)8\u3002\u8FD9\u79CD\u91D1\u5C5E\u7FB0\u57FA\u914D\u5408\u7269\u662F\u91D1\u5C5E\u6709\u673A\u5316\u5B66\u548C\u6709\u673A\u5408\u6210\u4E2D\u7684\u8BD5\u5242\u53CA\u50AC\u5316\u5242\u3002\u5B83\u88AB\u7528\u4E8E\u7FB0\u57FA\u5408\u6210\uFF0C\u4E5F\u5C31\u662F\u5C06\u70EF\u70C3\u8F6C\u5316\u6210\u919B\u7684\u50AC\u5316\u5242\u3002"@zh . . "Octacarbonyldicobalt(Co\u2014Co)"@en . "Dicobalt octacarbonyl, bridged C2v isomer"@en . . . "259200.0"^^ . . . "19576"^^ . "\u062B\u0645\u0627\u0646\u064A \u0643\u0631\u0628\u0648\u0646\u064A\u0644 \u062B\u0646\u0627\u0626\u064A \u0627\u0644\u0643\u0648\u0628\u0627\u0644\u062A \u0623\u0648 \u062B\u0645\u0627\u0646\u064A \u0643\u0631\u0628\u0648\u0646\u064A\u0644 \u0627\u0644\u0643\u0648\u0628\u0627\u0644\u062A \u0645\u0639\u0642\u062F \u0643\u0631\u0628\u0648\u0646\u064A\u0644 \u0644\u0647 \u0627\u0644\u0635\u064A\u063A\u0629 Co2(CO)8 \u060C \u0648\u064A\u0643\u0648\u0646 \u0639\u0644\u0649 \u0634\u0643\u0644 \u0628\u0644\u0648\u0631\u0627\u062A \u062D\u0645\u0631\u0627\u0621 \u0628\u0631\u062A\u0642\u0627\u0644\u064A\u0629."@ar . . . . . . . . . . . . . . . . . . . "L'octacarbonyle de dicobalt, ou plus simplement carbonyle de cobalt, est un compos\u00E9 chimique de formule Co2(CO)8. Ce carbonyle m\u00E9tallique est un r\u00E9actif et un catalyseur utilis\u00E9 en synth\u00E8se organique et en chimie des compos\u00E9s organom\u00E9talliques. Il a \u00E9t\u00E9 notamment utilis\u00E9 pour catalyser l'hydroformylation, conversion des alc\u00E8nes en ald\u00E9hydes."@fr . . . "\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB\u4E8C\u30B3\u30D0\u30EB\u30C8 (\u82F1: octacarbonyldicobalt) \u3068\u306F\u3001\u5206\u5B50\u5F0F\u304C Co2(CO)8 \u3068\u8868\u3055\u308C\u308B\u30B3\u30D0\u30EB\u30C8\u306E\u932F\u4F53\u306E\u4E00\u7A2E\u3002\u30B3\u30D0\u30EB\u30C8\u30AB\u30EB\u30DC\u30CB\u30EB\u3001\u4E8C\u30B3\u30D0\u30EB\u30C8\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB\u3001\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB\u30B8\u30B3\u30D0\u30EB\u30C8\u3001\u30B8\u30B3\u30D0\u30EB\u30C8\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB \u3068\u3082\u79F0\u3055\u308C\u308B\u3002\u6709\u6A5F\u91D1\u5C5E\u5316\u5B66\u3067\u8A66\u85AC\u3068\u3057\u3066\u7528\u3044\u3089\u308C\u3001\u95A2\u4FC2\u3059\u308B\u3044\u304F\u3064\u304B\u306E\u6709\u6A5F\u5408\u6210\u53CD\u5FDC\u304C\u77E5\u3089\u308C\u308B\u3002\u30D2\u30C9\u30ED\u30DB\u30EB\u30DF\u30EB\u5316\u53CD\u5FDC\u306E\u89E6\u5A92\u3068\u3057\u3066\u3082\u5229\u7528\u3055\u308C\u308B\u3002\u7D14\u5EA6\u306E\u9AD8\u3044\u7D50\u6676\u306F\u6A59\u8272\u3067\u3001\u7A7A\u6C17\u4E2D\u306B\u653E\u7F6E\u3059\u308B\u3068\u8910\u8272\u3092\u5E2F\u3073\u3001\u3055\u3089\u306B\u81EA\u7136\u767A\u706B\u3059\u308B\u3053\u3068\u304C\u3042\u308B\u3002\u6C34\u7D20\u3068\u4E00\u9178\u5316\u70AD\u7D20\u306E\u96F0\u56F2\u6C17\u4E2D\u3067\u306F\u5B89\u5B9A\u3067\u3042\u308B\u3002\u6C34\u306B\u4E0D\u6EB6\u3002"@ja . . . . . . "Oktakarbonyl dikobaltu je organokovov\u00E1 slou\u010Denina se vzorcem Co2(CO)8. Pou\u017E\u00EDv\u00E1 se jako reagent a katalyz\u00E1tor v organokovov\u00E9 chemii a organick\u00E9 synt\u00E9ze. Ka\u017Ed\u00E1 molekula sest\u00E1v\u00E1 ze dvou atom\u016F kobaltu, kter\u00E9 jsou v\u00E1zan\u00E9 k osmi karbonylov\u00FDm ligand\u016Fm, d\u00EDky tomu je zn\u00E1mo v\u00EDce strukturn\u00EDch izomer\u016F. N\u011Bkter\u00E9 karbonylov\u00E9 ligandy jsou velmi labiln\u00ED. Slou\u010Denina ochotn\u011B reaguje s alkyny a proto se n\u011Bkdy vyu\u017E\u00EDv\u00E1 jako chr\u00E1n\u00EDc\u00ED skupina."@cs . . "\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB\u4E8C\u30B3\u30D0\u30EB\u30C8 (\u82F1: octacarbonyldicobalt) \u3068\u306F\u3001\u5206\u5B50\u5F0F\u304C Co2(CO)8 \u3068\u8868\u3055\u308C\u308B\u30B3\u30D0\u30EB\u30C8\u306E\u932F\u4F53\u306E\u4E00\u7A2E\u3002\u30B3\u30D0\u30EB\u30C8\u30AB\u30EB\u30DC\u30CB\u30EB\u3001\u4E8C\u30B3\u30D0\u30EB\u30C8\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB\u3001\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB\u30B8\u30B3\u30D0\u30EB\u30C8\u3001\u30B8\u30B3\u30D0\u30EB\u30C8\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB \u3068\u3082\u79F0\u3055\u308C\u308B\u3002\u6709\u6A5F\u91D1\u5C5E\u5316\u5B66\u3067\u8A66\u85AC\u3068\u3057\u3066\u7528\u3044\u3089\u308C\u3001\u95A2\u4FC2\u3059\u308B\u3044\u304F\u3064\u304B\u306E\u6709\u6A5F\u5408\u6210\u53CD\u5FDC\u304C\u77E5\u3089\u308C\u308B\u3002\u30D2\u30C9\u30ED\u30DB\u30EB\u30DF\u30EB\u5316\u53CD\u5FDC\u306E\u89E6\u5A92\u3068\u3057\u3066\u3082\u5229\u7528\u3055\u308C\u308B\u3002\u7D14\u5EA6\u306E\u9AD8\u3044\u7D50\u6676\u306F\u6A59\u8272\u3067\u3001\u7A7A\u6C17\u4E2D\u306B\u653E\u7F6E\u3059\u308B\u3068\u8910\u8272\u3092\u5E2F\u3073\u3001\u3055\u3089\u306B\u81EA\u7136\u767A\u706B\u3059\u308B\u3053\u3068\u304C\u3042\u308B\u3002\u6C34\u7D20\u3068\u4E00\u9178\u5316\u70AD\u7D20\u306E\u96F0\u56F2\u6C17\u4E2D\u3067\u306F\u5B89\u5B9A\u3067\u3042\u308B\u3002\u6C34\u306B\u4E0D\u6EB6\u3002"@ja . . . . . "Dicobaltoctacarbonyl"@de . "changed"@en . . . "Dicobalt octacarbonyl"@en . . "\u516B\u7FB0\u57FA\u4E8C\u94B4"@zh . . . . "L'octacarbonyle de dicobalt, ou plus simplement carbonyle de cobalt, est un compos\u00E9 chimique de formule Co2(CO)8. Ce carbonyle m\u00E9tallique est un r\u00E9actif et un catalyseur utilis\u00E9 en synth\u00E8se organique et en chimie des compos\u00E9s organom\u00E9talliques. Il a \u00E9t\u00E9 notamment utilis\u00E9 pour catalyser l'hydroformylation, conversion des alc\u00E8nes en ald\u00E9hydes."@fr . . "Dicobalt octacarbonyl"@en . "6077160"^^ . . "1107867537"^^ . . . . . . . "\u041E\u043A\u0442\u0430\u043A\u0430\u0440\u0431\u043E\u043D\u0438\u043B\u0434\u0438\u043A\u043E\u0431\u0430\u043B\u044C\u0442 \u2014 \u043D\u0435\u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u0435 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0435, \u043A\u0430\u0440\u0431\u043E\u043D\u0438\u043B\u044C\u043D\u044B\u0439 \u043A\u043E\u043C\u043F\u043B\u0435\u043A\u0441 \u043A\u043E\u0431\u0430\u043B\u044C\u0442\u0430 \u0441\u043E\u0441\u0442\u0430\u0432\u0430 Co2(CO)8. \u041A\u0440\u0430\u0441\u043D\u043E-\u043E\u0440\u0430\u043D\u0436\u0435\u0432\u044B\u0435 \u043A\u0440\u0438\u0441\u0442\u0430\u043B\u043B\u044B, \u043D\u0435 \u0440\u0430\u0441\u0442\u0432\u043E\u0440\u0438\u043C\u044B\u0435 \u0432 \u0432\u043E\u0434\u0435."@ru . "Dicobalt octacarbonyl is an organocobalt compound with composition Co2(CO)8. This metal carbonyl is used as a reagent and catalyst in organometallic chemistry and organic synthesis, and is central to much known organocobalt chemistry. It is the parent member of a family of hydroformylation catalysts. Each molecule consists of two cobalt atoms bound to eight carbon monoxide ligands, although multiple structural isomers are known. Some of the carbonyl ligands are labile."@en . . . . . . . . . . . . . . . . "\u516B\u7FB0\u57FA\u4E8C\u94B4\u662F\u4E00\u79CD\u65E0\u673A\u5316\u5408\u7269\uFF0C\u5316\u5B66\u5F0F\u4E3ACo2(CO)8\u3002\u8FD9\u79CD\u91D1\u5C5E\u7FB0\u57FA\u914D\u5408\u7269\u662F\u91D1\u5C5E\u6709\u673A\u5316\u5B66\u548C\u6709\u673A\u5408\u6210\u4E2D\u7684\u8BD5\u5242\u53CA\u50AC\u5316\u5242\u3002\u5B83\u88AB\u7528\u4E8E\u7FB0\u57FA\u5408\u6210\uFF0C\u4E5F\u5C31\u662F\u5C06\u70EF\u70C3\u8F6C\u5316\u6210\u919B\u7684\u50AC\u5316\u5242\u3002"@zh . . . . "\u30AA\u30AF\u30BF\u30AB\u30EB\u30DC\u30CB\u30EB\u4E8C\u30B3\u30D0\u30EB\u30C8"@ja . . . "438551689"^^ . . "Dicobalt-octacarbonyl-C2v-bridged-from-xtal-1983-3D-balls-A.png"@en . . "Dicobaltoctacarbonyl ist ein zweikerniger Komplex, bei dem zwei Cobaltkerne von acht Carbonylliganden umgeben sind."@de . . . . "Dikobaltoctacarbonyl is het anorganische kobaltverbinding met als formule Co2(CO)8. De stof komt voor als oranje kristallen, die onoplosbaar zijn in water. De stof is pyrofoor."@nl . . . "Octacarbonyle de dicobalt"@fr . "Octacarbonyldicobalt"@en . . . . . "Cobalt carbonyl (2:8), di-mu-Carbonylhexacarbonyldicobalt, Cobalt octacarbonyl, Cobalt tetracarbonyl dimer, Dicobalt carbonyl, Octacarbonyldicobalt"@en . . . . . . . . . "\u041E\u043A\u0442\u0430\u043A\u0430\u0440\u0431\u043E\u043D\u0438\u043B\u0434\u0438\u043A\u043E\u0431\u0430\u043B\u044C\u0442"@ru . . . . . "Octacarbonilo de dicobalto"@es . "Oktakarbonyl dikobaltu"@cs . . "Dikobaltoctacarbonyl"@nl . . . . . . "\u041E\u043A\u0442\u0430\u043A\u0430\u0440\u0431\u043E\u043D\u0438\u043B\u0434\u0438\u043A\u043E\u0431\u0430\u043B\u044C\u0442 \u2014 \u043D\u0435\u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u0435 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0435, \u043A\u0430\u0440\u0431\u043E\u043D\u0438\u043B\u044C\u043D\u044B\u0439 \u043A\u043E\u043C\u043F\u043B\u0435\u043A\u0441 \u043A\u043E\u0431\u0430\u043B\u044C\u0442\u0430 \u0441\u043E\u0441\u0442\u0430\u0432\u0430 Co2(CO)8. \u041A\u0440\u0430\u0441\u043D\u043E-\u043E\u0440\u0430\u043D\u0436\u0435\u0432\u044B\u0435 \u043A\u0440\u0438\u0441\u0442\u0430\u043B\u043B\u044B, \u043D\u0435 \u0440\u0430\u0441\u0442\u0432\u043E\u0440\u0438\u043C\u044B\u0435 \u0432 \u0432\u043E\u0434\u0435."@ru . . . . "El octacarbonilo de dicobalto es el compuesto inorg\u00E1nico Co2(CO)8. Este carbonilo met\u00E1lico es un reactivo y catalizador usado en qu\u00EDmica organomet\u00E1lica y s\u00EDntesis org\u00E1nica.\u200B Se utiliza como catalizador para la reacci\u00F3n de hidroformilaci\u00F3n (conversi\u00F3n de alquenos en aldeh\u00EDdos).\u200B"@es . . . . .