{"title":"零价钌的异氰化物配合物。质子添加到过渡金属碱中，提供替代的碱基位置","authors":"D. F. Christian, W. R. Roper","doi":"10.1039/C29710001271","DOIUrl":null,"url":null,"abstract":"Ru(CO)2(CNR)(PPh3)2, Ru(CO)(CNR)(PPh3)3, and the dioxygen complex Ru(O2)(CO)(CNR)(PPh3)2, (R =p-tolyl) have been prepared by the action of bases on [RuH(CO)2(CNR)(PPh3)2]+ and [RuH(CO)(CNR)-(PPh3)3]+; protonation of Ru(CO)2(CNR)(PPh3)2 occurs specifically trans to isocyanide.","PeriodicalId":17278,"journal":{"name":"Journal of The Chemical Society D: Chemical Communications","volume":"345 1","pages":"1271-1272"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"17","resultStr":"{\"title\":\"Isocyanide complexes of zerovalent ruthenium. Proton addition to a transition-metal base offering alternative base sites\",\"authors\":\"D. F. Christian, W. R. Roper\",\"doi\":\"10.1039/C29710001271\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ru(CO)2(CNR)(PPh3)2, Ru(CO)(CNR)(PPh3)3, and the dioxygen complex Ru(O2)(CO)(CNR)(PPh3)2, (R =p-tolyl) have been prepared by the action of bases on [RuH(CO)2(CNR)(PPh3)2]+ and [RuH(CO)(CNR)-(PPh3)3]+; protonation of Ru(CO)2(CNR)(PPh3)2 occurs specifically trans to isocyanide.\",\"PeriodicalId\":17278,\"journal\":{\"name\":\"Journal of The Chemical Society D: Chemical Communications\",\"volume\":\"345 1\",\"pages\":\"1271-1272\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"17\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society D: Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/C29710001271\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society D: Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/C29710001271","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Isocyanide complexes of zerovalent ruthenium. Proton addition to a transition-metal base offering alternative base sites
Ru(CO)2(CNR)(PPh3)2, Ru(CO)(CNR)(PPh3)3, and the dioxygen complex Ru(O2)(CO)(CNR)(PPh3)2, (R =p-tolyl) have been prepared by the action of bases on [RuH(CO)2(CNR)(PPh3)2]+ and [RuH(CO)(CNR)-(PPh3)3]+; protonation of Ru(CO)2(CNR)(PPh3)2 occurs specifically trans to isocyanide.
京公网安备 11010802042870号
京ICP备2023020795号-1
分享
求助内容：
应助结果提醒方式：
扫码关注我们
