Metallacarboranes containing carborane ligands possessing a pentagonal open face can coordinate metal atoms in a η5-manner quite similar to the cyclopentadienyl monoanion, thus affording metallocene analogues. By virtue of such an analogy, their electron transfer aptitude plays an important role in their physico-chemical characterisation. We review such an aspect, also providing evidence for the structural consequences of their electron transfer processes. At variance with metallocenes, electrochemical investigations on the metallacarboranes have not yet become a routine tool to search for their potential application in fields which require electronic mobility
The preferred structure of 12-vertex, 28-electron (nido) polyhedral cages, which contain two skeleta...
Alkane elimination reaction of Hf(CH2SiMe3) 4 with a zwitterionic salt 1-Me2NHCH2CH2 -1,3-C2B10H12 h...
The formation of icosahedral carboranes, their degradation to dicarbollide ions, and formation of me...
Metallacarboranes containing carborane ligands possessing a pentagonal open face can coordinate meta...
Ten years after the discovery of metallocarboranes, this field of chemistry is still advancing at a ...
The properties of some new metallacarboranes are described in this thesis, along with the results of...
Ferrocene and its derivatives have been extensively used as an internal reference in electrochemical...
A series of metallacarboranes, incorporating the CpFe fragment, were studied by electrochemical tech...
Electronic interactions and metal−metal communication in a wide range of cobaltacarborane−hydrocarbo...
The goal of this dissertation was to further investigate reactions and the metal coordination proper...
With the goal to produce molecules with high electron accepting capacity and low reorganization ener...
A cohesive notation for indicating the overall number of electrons associated with metallaboratanes ...
Chapter 1 presents the most relevant literature in the fields of borane, carborane and metallacarbor...
Abstract: This article provides an overview of our work on the synthesis, molecular structure, and b...
The reactions of [RuCl(Cp*)]4 with monoanionic, charge-compensated carborane anions have been studie...
The preferred structure of 12-vertex, 28-electron (nido) polyhedral cages, which contain two skeleta...
Alkane elimination reaction of Hf(CH2SiMe3) 4 with a zwitterionic salt 1-Me2NHCH2CH2 -1,3-C2B10H12 h...
The formation of icosahedral carboranes, their degradation to dicarbollide ions, and formation of me...
Metallacarboranes containing carborane ligands possessing a pentagonal open face can coordinate meta...
Ten years after the discovery of metallocarboranes, this field of chemistry is still advancing at a ...
The properties of some new metallacarboranes are described in this thesis, along with the results of...
Ferrocene and its derivatives have been extensively used as an internal reference in electrochemical...
A series of metallacarboranes, incorporating the CpFe fragment, were studied by electrochemical tech...
Electronic interactions and metal−metal communication in a wide range of cobaltacarborane−hydrocarbo...
The goal of this dissertation was to further investigate reactions and the metal coordination proper...
With the goal to produce molecules with high electron accepting capacity and low reorganization ener...
A cohesive notation for indicating the overall number of electrons associated with metallaboratanes ...
Chapter 1 presents the most relevant literature in the fields of borane, carborane and metallacarbor...
Abstract: This article provides an overview of our work on the synthesis, molecular structure, and b...
The reactions of [RuCl(Cp*)]4 with monoanionic, charge-compensated carborane anions have been studie...
The preferred structure of 12-vertex, 28-electron (nido) polyhedral cages, which contain two skeleta...
Alkane elimination reaction of Hf(CH2SiMe3) 4 with a zwitterionic salt 1-Me2NHCH2CH2 -1,3-C2B10H12 h...
The formation of icosahedral carboranes, their degradation to dicarbollide ions, and formation of me...