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Gemma Barberà | doi.page

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Gemma Barberà

Consejo Superior de Investigaciones Científicas(ES)Institut de Ciència de Materials de Barcelona(ES)

Publications by Year

Research Areas

Boron Compounds in Chemistry, Radioactive element chemistry and processing, Radiopharmaceutical Chemistry and Applications, Crystallography and molecular interactions, Crystallization and Solubility Studies

Most-Cited Works

→ Are Methyl Groups Electron-Donating or Electron-Withdrawing in Boron Clusters? Permethylation of o-Carborane(2005)215 cited
→ Are Halocarboranes Suitable for Substitution Reactions? The Case for 3-I-1,2-closo-C₂B₁₀H₁₁: Molecular Orbital Calculations, Aryldehalogenation Reactions, 11B NMR Interpretation of closo-Carboranes, and Molecular Structures of 1-Ph-3-Br-1,2-closo-C₂B₁₀H₁₀ and 3-Ph-1,2-closo-C₂B₁₀H₁₁(2001)97 cited
→ Designed Synthesis of New ortho-Carborane Derivatives: from Mono- to Polysubstituted Frameworks(2008)72 cited
→ Synthesis of Boron-Iodinated o-Carborane Derivatives. Water Stability of the Periodinated Monoprotic Salt(2006)59 cited
→ Self-assembly of carborane molecules via C–H⋯I hydrogen bonding: the molecular and crystal structures of 3-I-1,2-closo-C₂B₁₀H₁₁(2002)55 cited

→ From Mono‐ to Poly‐Substituted Frameworks: A Way of Tuning the Acidic Character of C_cH in o‐Carborane Derivatives(2009)

45 cited

→ The BI activation in o-carborane clusters: their fate towards BH. Easy synthesis of [7,10-C2B10H13]−(2002)34 cited

→ High yield [125I]iodide-labeling of iodinated carboranes by palladium-catalyzed isotopic exchange(2003)27 cited

→ Sequential Nucleophilic−Electrophilic Reactions Selectively Produce Isomerically Pure Nona‐B‐Substituted o‐Carborane Derivatives(2003)25 cited

→ Retention of the B(3)X (X=Br, I) bond in closo-o-carborane derivatives after nucleophilic attack. The first synthesis of [3-X-7-R-7,8-nido-C2B9H10]− (X=Br, I). Crystal structure of [HNMe3][3-I-7,8-nido-C2B9H11](2002)22 cited