- Interactions between carboranethiols and metal (Au/Ag/Cu) surfaces.
- Boron hydride clusters as building blocks for 2-D and 3-D molecular assemblies.
- Au single crystals and various other dimensional levels of gold
Publications
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] Type Year Filters: First Letter Of Last Name is B [Clear All Filters]
. Carboranethiols: Building Blocks for Self-Assembled Monolayers on Copper Surfaces, or a Novel Class of Etchants?. European Materials Research Society, Spring Meeting. 2012.
e-mrs_springmeeting_2012_t_base_poster.pdf (646.88 KB) e-mrs_springeeting_2012_t_base_abstract.pdf (16.55 KB)
e-mrs_springmeeting_2012_t_base_poster.pdf (646.88 KB) e-mrs_springeeting_2012_t_base_abstract.pdf (16.55 KB) Carborane-thiol-silver interactions. A comparative study of the molecular protection of silver surfaces. Surface and Coatings Technology. 2010;204. Available at: http://www.sciencedirect.com/science/article/pii/S0257897210001106.
Carborane-thiol-silver interactions. A comparative study of the molecular protection of silver surfaces. Surface and Coatings Technology. 2010;204. Available at: http://www.sciencedirect.com/science/article/pii/S0257897210001106.
Carborane-thiol-silver interactions. A comparative study of the molecular protection of silver surfaces. Surface and Coatings Technology. 2010;204. Available at: http://www.sciencedirect.com/science/article/pii/S0257897210001106.
. Chemie podivnych tvaru aneb Vylet do rise hydridu boru (in Czech). Vesmir. 2008;87:748-749. Available at: http://casopis.vesmir.cz/clanky/clanek/id/8022. base_londesborough_vesmir_2008-11_vol87_pp748-749.pdf (175.89 KB)
base_londesborough_vesmir_2008-11_vol87_pp748-749.pdf (175.89 KB). A comparison of boron hydride- and hydrocarbon-based thiol derivatives assembled on gold surfaces. NSTI Nanotechnology Conference and Trade Show. 2008;1. Available at: http://www.nsti.org/procs/Nanotech2008v1/2/T35.902.
. A comparison of boron hydride- and hydrocarbon-based thiol derivatives assembled on gold surfaces. NSTI Nanotechnology Conference and Trade Show. 2008;1. Available at: http://www.nsti.org/procs/Nanotech2008v1/2/T35.902.
Competing Intermolecular and Molecule–Surface Interactions: Dipole–Dipole-Driven Patterns in Mixed Carborane Self-Assembled Monolayers. Chemistry of Materials. 2024;36:2085-2095. Available at: https://pubs.acs.org/doi/10.1021/acs.chemmater.3c03210.
Competing Intermolecular and Molecule–Surface Interactions: Dipole–Dipole-Driven Patterns in Mixed Carborane Self-Assembled Monolayers. Chemistry of Materials. 2024;36:2085-2095. Available at: https://pubs.acs.org/doi/10.1021/acs.chemmater.3c03210.
Decaborane Thiols as Building Blocks for Self-Assembled Monolayers on Metal Surfaces. Inorganic Chemistry. 2012;51.
Decaborane Thiols as Building Blocks for Self-Assembled Monolayers on Metal Surfaces. Inorganic Chemistry. 2012;51.
Decaborane Thiols as Building Blocks for Self-Assembled Monolayers on Metal Surfaces. Inorganic Chemistry. 2012;51.
. Effizienter Korrosionsschutz von Silberoberflächen durch eine schonende und einfache molekulare Technologie. Horizonte. 2016;(47):24-28. Available at: http://www.koord.hs-mannheim.de/deutsch/horizonte.html.
An Experimental Solution to the "Missing Hydrogens" Question Surrounding the Macropolyhedral 19-Vertex Boron Hydride Monoanion [B19H22](-), a Simplification of Its Synthesis, and Its Use As an Intermediate in the First Example of syn-B18H22 to anti-B18H22. Inorganic Chemistry. 2010;49(9). Available at: http://pubs.acs.org/doi/abs/10.1021/ic901976y.
An Experimental Solution to the "Missing Hydrogens" Question Surrounding the Macropolyhedral 19-Vertex Boron Hydride Monoanion [B19H22](-), a Simplification of Its Synthesis, and Its Use As an Intermediate in the First Example of syn-B18H22 to anti-B18H22. Inorganic Chemistry. 2010;49(9). Available at: http://pubs.acs.org/doi/abs/10.1021/ic901976y.
An Experimental Solution to the "Missing Hydrogens" Question Surrounding the Macropolyhedral 19-Vertex Boron Hydride Monoanion [B19H22](-), a Simplification of Its Synthesis, and Its Use As an Intermediate in the First Example of syn-B18H22 to anti-B18H22. Inorganic Chemistry. 2010;49(9). Available at: http://pubs.acs.org/doi/abs/10.1021/ic901976y.
Formation of Highly Ordered Terminal Alkyne Self-Assembled Monolayers on the Au{111} Surface through Substitution of 1-Decaboranethiolate. J. Phys. Chem. C. 2019;123(2):1348–1353. Available at: https://pubs.acs.org/doi/10.1021/acs.jpcc.8b11033.
. The gaseous structure of closo-9,12-(SH)2-1,2-C2B10H10, a modifier of gold surfaces, as determined using electron diffraction and computational methods. Dalton Transactions. 2013;42. Available at: http://pubs.rsc.org/en/results?artrefjournalname=dalton%20trans.&artrefstartpage=12015&artrefvolumeyear=2013&fcategory=journal.
Gold Micrometer Crystals Modified with Carboranethiol Derivatives. J. Phys. Chem. C. 2008;112(37). Available at: http://pubs.acs.org/doi/abs/10.1021/jp802281s.
Gold Micrometer Crystals Modified with Carboranethiol Derivatives. J. Phys. Chem. C. 2008;112(37). Available at: http://pubs.acs.org/doi/abs/10.1021/jp802281s.
Icosahedral Carbaboranes with Peripheral Hydrogen– Chalcogenide Groups: Structures from Gas Electron Diffraction and Chemical Shielding in Solution. Chemistry A European Journal. 2019;25(9):2313-2321. Available at: https://onlinelibrary.wiley.com/doi/10.1002/chem.201805145.
Influence of Terminal Carboxyl Group on Structure and Reactivity of Functionalized m-Carboranethiolate Self-Assembled Monolayers. Chemistry of Materials. 2020;32:6800−6809. Available at: https://pubs.acs.org/doi/10.1021/acs.chemmater.0c02722.
Influence of Terminal Carboxyl Group on Structure and Reactivity of Functionalized m-Carboranethiolate Self-Assembled Monolayers. Chemistry of Materials. 2020;32:6800−6809. Available at: https://pubs.acs.org/doi/10.1021/acs.chemmater.0c02722.
. Klastrové molekuly na površích substrátů (in Czech only). Scientific American (Czech edition). 2017;květen_2017:34-35. Available at: http://www.sciam.cz/files/UACH_5-2017_web.pdf. base_scientificamerican_2017_spec-sekce_uach_5-2017_web.pdf (394.57 KB)
base_scientificamerican_2017_spec-sekce_uach_5-2017_web.pdf (394.57 KB) Light-Activated Intercluster Conversion of an Atomically Precise Silver Nanocluster. ACS Nano. 2021;15(10):15781-15793. Available at: https://pubs.acs.org/doi/abs/10.1021/acsnano.1c02602.
