A new series of bifunctional Ru complexes with pendent Lewis acidic boranes were prepared by late-stage modification of an active hydrogen-transfer catalyst. The appended boranes modulate the reactivity of a metal hydride as well as catalytic hydrogenations. After installing acidic auxiliary groups, the complexes become multifunctional and catalyze the cis-selective hydrogenation of alkynes with higher rates, conversions, and selectivities compared with the unmodified catalyst
[[abstract]]Using an exchange reaction involving one PCy3 ligand in HRu(CO)Cl(PCy3)2 (1) for one IMe...
A series of bimetallic N-heterocyclic carbene Rh(I) complexes (<b>13</b>, <b>14</b>, <b>16</b>, <b>...
A catalyst loading of between 0.001–0.05 mol% of the PNN-bearing ruthenium(II) complex [fac-PNN]RuH(...
Reactions of internal alkynes with R<sub>3</sub>M–H (M = Si, Ge, Sn) follow an unconventional trans-...
By the introduction of −OH group(s) into different position(s) of 6-(pyridin-2-ylmethyl)-2,2′-bipyri...
The nonclassical ruthenium hydride pincer complex [Ru(PNP)(H)<sub>2</sub>(H<sub>2</sub>)] <b>1</b>...
In contrast to all other transition-metal-catalyzed hydrostannation reactions documented in the lite...
Reversible, heterolytic addition of H<sub>2</sub> across an iron–boron bond in a ferraboratrane with...
Reactions of internal alkynes with R<sub>3</sub>M–H (M = Si, Ge, Sn) follow an unconventional <i>tra...
Recently, the Furstner group reported the first general trans-hydroboration of internal alkynes by u...
Remarkable differences in selectivity and activity for ruthenium-catalyzed transfer hydrogenation ar...
The purpose of the thesis is the catalyzed functionalization of alkynes, alkenes and arenes via hydr...
The synthesis, characterization and catalytic activity of a new class of diruthenium hydrido carbony...
In addition to our previous works for PBP-pincer metal complexes, four PBP-pincer Ru complexes, [PBP...
Three unsymmetrical NNN ligands with a 2-hydroxypyridyl fragment were used to react with RuHCl(PPh3...
[[abstract]]Using an exchange reaction involving one PCy3 ligand in HRu(CO)Cl(PCy3)2 (1) for one IMe...
A series of bimetallic N-heterocyclic carbene Rh(I) complexes (<b>13</b>, <b>14</b>, <b>16</b>, <b>...
A catalyst loading of between 0.001–0.05 mol% of the PNN-bearing ruthenium(II) complex [fac-PNN]RuH(...
Reactions of internal alkynes with R<sub>3</sub>M–H (M = Si, Ge, Sn) follow an unconventional trans-...
By the introduction of −OH group(s) into different position(s) of 6-(pyridin-2-ylmethyl)-2,2′-bipyri...
The nonclassical ruthenium hydride pincer complex [Ru(PNP)(H)<sub>2</sub>(H<sub>2</sub>)] <b>1</b>...
In contrast to all other transition-metal-catalyzed hydrostannation reactions documented in the lite...
Reversible, heterolytic addition of H<sub>2</sub> across an iron–boron bond in a ferraboratrane with...
Reactions of internal alkynes with R<sub>3</sub>M–H (M = Si, Ge, Sn) follow an unconventional <i>tra...
Recently, the Furstner group reported the first general trans-hydroboration of internal alkynes by u...
Remarkable differences in selectivity and activity for ruthenium-catalyzed transfer hydrogenation ar...
The purpose of the thesis is the catalyzed functionalization of alkynes, alkenes and arenes via hydr...
The synthesis, characterization and catalytic activity of a new class of diruthenium hydrido carbony...
In addition to our previous works for PBP-pincer metal complexes, four PBP-pincer Ru complexes, [PBP...
Three unsymmetrical NNN ligands with a 2-hydroxypyridyl fragment were used to react with RuHCl(PPh3...
[[abstract]]Using an exchange reaction involving one PCy3 ligand in HRu(CO)Cl(PCy3)2 (1) for one IMe...
A series of bimetallic N-heterocyclic carbene Rh(I) complexes (<b>13</b>, <b>14</b>, <b>16</b>, <b>...
A catalyst loading of between 0.001–0.05 mol% of the PNN-bearing ruthenium(II) complex [fac-PNN]RuH(...