1998
DOI: 10.1002/(sici)1521-3757(19980518)110:10<1481::aid-ange1481>3.0.co;2-6
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Ein überraschendes Addukt einescloso-Clusters

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Cited by 3 publications
(2 citation statements)
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“…In order to isolate quantitatively the dimethylamide adduct of 1 an excess of amide was used. In the case of the methyl substituted silaborane an adduct with dimethylamide and diethylamide is formed [8]. As a result of the larger phenyl substituents the closo cluster 1 is only able to form an adduct with the smaller dimethylamide nucleophile.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In order to isolate quantitatively the dimethylamide adduct of 1 an excess of amide was used. In the case of the methyl substituted silaborane an adduct with dimethylamide and diethylamide is formed [8]. As a result of the larger phenyl substituents the closo cluster 1 is only able to form an adduct with the smaller dimethylamide nucleophile.…”
Section: Resultsmentioning
confidence: 99%
“…(Scheme 2) Hawthorne postulated the formation of an adduct between the attacking nucleophile and the closo cluster as the first step in a mechanistic sequence for the nucleophilic degradation of o-carborane [7]. In the case of 1,2-dimethyl-o-silaborane we had been able to isolate and characterize an adduct between the nucleophile diethylamide and the closo cluster 2 [8]. (Scheme 3) This adduct exhibits the structure of a closo cluster with an arachno electron household.…”
Section: Resultsmentioning
confidence: 99%