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F Teixidor

Showing results (11-20 of 15) with videos related to

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Dalton Transactions (Cambridge, England : 2003)|April 17, 2008
Synthesis, reactivity and complexation studies of N,S exo-heterodisubstituted o-carborane ligands. Carborane as a platform to produce the uncommon bidentate chelating (pyridine)N-C-C-C-s(H) motifF Teixidor, A Laromaine, R Kivekäs, et al.
Inorganic Chemistry|December 12, 2001
Are halocarboranes suitable for substitution reactions? The case for 3-I-1,2-closo-C(2)B(10)H(11): molecular orbital calculations, aryldehalogenation reactions, (11)B NMR interpretation of closo-carboranes, and molecular structures of 1-Ph-3-Br-1,2-closo-C(2)B(10)H(10) and 3-Ph-1,2-closo-C(2)B(10)H(11)C Viñas, G Barberà, J M Oliva, et al.
Inorganic Chemistry|February 24, 2001
Unusual 9-->10 rearrangement of the substituted cage carbon in the ferratricarbollide series. Synthesis of the isomeric complexes [2-eta 5-(C5H5)-10-X-closo-2,1,7,10-FeC3B8H10] (where X = H2N, MeHN, Me2N, and ButHN)B Grüner, A Lehtonen, R Kivekäs, et al.
Nanoscale|April 22, 2025
Cobaltabis(dicarbollide) [<i>o</i>-COSAN]<sup>-</sup> loaded apoferritin: an innovative high-capacity boron delivery system to target tumour cells for BNCT applicationsD Alberti, J N Piña Marcos, S Rakhshan, et al.
Dalton Transactions (Cambridge, England : 2003)|January 4, 2017
Carborane-stilbene dyads: the influence of substituents and cluster isomers on photoluminescence propertiesA Ferrer-Ugalde, J Cabrera-González, E J Juárez-Pérez, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Dalton Transactions (Cambridge, England : 2003)|April 17, 2008
Synthesis, reactivity and complexation studies of N,S exo-heterodisubstituted o-carborane ligands. Carborane as a platform to produce the uncommon bidentate chelating (pyridine)N-C-C-C-s(H) motifF Teixidor, A Laromaine, R Kivekäs, et al.
Inorganic Chemistry|December 12, 2001
Are halocarboranes suitable for substitution reactions? The case for 3-I-1,2-closo-C(2)B(10)H(11): molecular orbital calculations, aryldehalogenation reactions, (11)B NMR interpretation of closo-carboranes, and molecular structures of 1-Ph-3-Br-1,2-closo-C(2)B(10)H(10) and 3-Ph-1,2-closo-C(2)B(10)H(11)C Viñas, G Barberà, J M Oliva, et al.
Inorganic Chemistry|February 24, 2001
Unusual 9-->10 rearrangement of the substituted cage carbon in the ferratricarbollide series. Synthesis of the isomeric complexes [2-eta 5-(C5H5)-10-X-closo-2,1,7,10-FeC3B8H10] (where X = H2N, MeHN, Me2N, and ButHN)B Grüner, A Lehtonen, R Kivekäs, et al.
Nanoscale|April 22, 2025
Cobaltabis(dicarbollide) [<i>o</i>-COSAN]<sup>-</sup> loaded apoferritin: an innovative high-capacity boron delivery system to target tumour cells for BNCT applicationsD Alberti, J N Piña Marcos, S Rakhshan, et al.
Dalton Transactions (Cambridge, England : 2003)|January 4, 2017
Carborane-stilbene dyads: the influence of substituents and cluster isomers on photoluminescence propertiesA Ferrer-Ugalde, J Cabrera-González, E J Juárez-Pérez, et al.
Pageof 2