Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Braulio M. Puerta Lombardi"'
Autor:
Braulio M. Puerta Lombardi, Morgan R. Faas, Daniel West, Roope A. Suvinen, Heikki M. Tuononen, Roland Roesler
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-7 (2024)
Abstract Chelating ligands have had a tremendous impact in coordination chemistry and catalysis. Notwithstanding their success as strongly σ-donating and π-accepting ligands, to date no chelating bis[cyclic (alkyl)(amino)carbenes] have been reporte
Externí odkaz:
https://doaj.org/article/a4a4f1ec1e084d9da1ebd9cff24a67f0
Autor:
Jan-Erik Siewert, Braulio M. Puerta Lombardi, Nora Janssen, Roland Roesler, Christian Hering-Junghans
N-heterocyclic carbene-phosphinidene adducts (NHPs) are an emerging class of ligands with proven binding ability for main group and transition elements. They can be considered as inversely polarized phosphaalkenes with electron-rich P atoms possessin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a383a363010c46bb00f5daba7d16747
https://doi.org/10.26434/chemrxiv-2023-1f1ct
https://doi.org/10.26434/chemrxiv-2023-1f1ct
Autor:
Braulio M, Puerta Lombardi, Ethan R, Pezoulas, Roope A, Suvinen, Alexander, Harrison, Zachary S, Dubrawski, Benjamin S, Gelfand, Heikki M, Tuononen, Roland, Roesler
Publikováno v:
Chemical communications (Cambridge, England). 58(45)
Isomeric bis(aldiminium) salts with a 1,4-cyclohexylene framework were synthesized. The first isolable bis(CAAC) was prepared from the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3ee47063bbcfa4082a1747d94778b18
https://pubmed.ncbi.nlm.nih.gov/35583166
https://pubmed.ncbi.nlm.nih.gov/35583166
Autor:
Roland Roesler, Sathish Ponnurangam, Zachary S. Dubrawski, Chase L. Radford, Janina Willkomm, Alexander S. Hyla, Joshua Heidebrecht, Gregory C. Welch, Jian-Bin Lin, Warren E. Piers, Braulio M. Puerta Lombardi, Demyan E. Prokopchuk
Publikováno v:
Sustainable Energy & Fuels. 3:1172-1181
We report the synthesis of Ni(TAPPy)2 (TAPPy = 1,3,5-triazapentadienyl-2,4-bis(2-pyridyl)) and its reactivity with CO2 under reducing conditions. Electrochemical reduction of Ni(TAPPy)2 under inert gas reveals that the complex accommodates up to two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65d9e7ae14f67b31b329f9c69c99dc8a
https://doi.org/10.1039/c8se00623g
https://doi.org/10.1039/c8se00623g
Autor:
Chia Yun Chang, Braulio M. Puerta Lombardi, Rudy M. Brown, Tristram Chivers, Chris Gendy, Roland Roesler
Publikováno v:
Organometallics. 36:3250-3256
This work explores avenues toward PCP pincer complexes with acyclic diaminocarbene central moieties that are suitable for ligand-assisted reactivity involving the carbene carbon. For this purpose, diphosphine chelating ligands 1 and 2, with bis(imida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::819f16323c952f23bc3166d1f5dc7283
https://doi.org/10.1021/acs.organomet.7b00396
https://doi.org/10.1021/acs.organomet.7b00396
Autor:
Zachary Dubrawski, Joshua E. Heidebrecht, Braulio M. Puerta Lombardi, Alexander Hyla, Janina Willkomm, Chase Radford, Jian-Bin Li, Gregory C. Welch, Sathish Ponnurangam, Roland Roesler, Demyan E. Prokopchuk, Warren Piers
We report the synthesis of Ni(TAPPy)2 (TAPPy = 1,3,5-triazapentadienyl-2,4-bis(2-pyridyl)) and its reactivity with CO2 under reducing conditions. Electrochemical reduction of Ni(TAPPy)2 under inert gas reveals that the complex accommodates up to two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::119ff29a213bb2b0c24bd4471c0a3dae
https://doi.org/10.26434/chemrxiv.7479665.v1
https://doi.org/10.26434/chemrxiv.7479665.v1
Autor:
Braulio M. Puerta Lombardi, Ethan R. Pezoulas, Roope A. Suvinen, Alexander Harrison, Zachary S. Dubrawski, Benjamin S. Gelfand, Heikki M. Tuononen, Roland Roesler
Publikováno v:
Chemical Communications. 58(45):6482-6485
A trans-bis(CAAC) was isolated and shown to be a ditopic ligand for rhodium and iridium. The cis-isomer is unstable towards intramolecular CC-bond formation, however, its formal insertion products into the bonds of H2O and NH3 were identified.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f36dcebff950699604a2048f46c744
Autor:
'Braulio M. Puerta Lombardi
Publikováno v:
Ethan R. Pezoulas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r3c4b2081b22::37aec816c63a6d1c349a9aec7b8408d4