@article{MTMT:34546230,
	title = {THE TALE OF ALKYL- AND ACYLCOBALT CARBONYLS,},
	url = {https://m2.mtmt.hu/api/publication/34546230},
	author = {Tuba, Róbert and Kurdi, Róbert and Pályi, Gyula},
	doi = {10.1016/j.jorganchem.2024.123029},
	journal-iso = {J ORGANOMET CHEM},
	journal = {JOURNAL OF ORGANOMETALLIC CHEMISTRY},
	volume = {.2024},
	unique-id = {34546230},
	issn = {0022-328X},
	year = {2024},
	eissn = {1872-8561},
	pages = {123029-123055},
	orcid-numbers = {Kurdi, Róbert/0000-0002-7845-2045}
}

@{MTMT:33833364,
	title = {Catalysts system and process for the preparation of alpha olefins and alpha olefin-containing products from long-chain paraffins},
	url = {https://m2.mtmt.hu/api/publication/33833364},
	author = {Tuba, Róbert and Valyon, József and Hancsók, Jenő and Lónyi, Ferenc and Tomasek, Szabina and Nagyházi, Márton and Miskolczi, Norbert and Horváth, D. Z. and Vikár, Anna and Balla, Á.},
	unique-id = {33833364},
	year = {2023},
	orcid-numbers = {Valyon, József/0000-0002-3608-060X; Hancsók, Jenő/0000-0003-1959-7604; Tomasek, Szabina/0000-0003-1947-5690; Miskolczi, Norbert/0000-0003-4862-0148; Vikár, Anna/0000-0002-3069-3034}
}

@article{MTMT:33779022,
	title = {Making Persistent Plastics Degradable},
	url = {https://m2.mtmt.hu/api/publication/33779022},
	author = {Farkas, Vajk and Nagyházi, Márton and Anastas, Paul T. and Klankermayer, Jürgen and Tuba, Róbert},
	doi = {10.1002/cssc.202300553},
	journal-iso = {CHEMSUSCHEM},
	journal = {CHEMSUSCHEM},
	volume = {16},
	unique-id = {33779022},
	issn = {1864-5631},
	year = {2023},
	eissn = {1864-564X},
	orcid-numbers = {Farkas, Vajk/0000-0002-1189-0032}
}

@{MTMT:33833358,
	title = {Katalizátorrendszer és eljárás alfa-olefinek és alfa-olefin-tartalmú termékek előállítására hosszú szénláncú paraffinokból},
	url = {https://m2.mtmt.hu/api/publication/33833358},
	author = {Tuba, Róbert and Valyon, József and Hancsók, Jenő and Lónyi, Ferenc and Tomasek, Szabina and Nagyházi, Márton and Miskolczi, Norbert and Horváth, D. Z. and Vikár, Anna and Balla, Á.},
	unique-id = {33833358},
	year = {2022},
	orcid-numbers = {Valyon, József/0000-0002-3608-060X; Hancsók, Jenő/0000-0003-1959-7604; Tomasek, Szabina/0000-0003-1947-5690; Miskolczi, Norbert/0000-0003-4862-0148; Vikár, Anna/0000-0002-3069-3034}
}

@article{MTMT:33262683,
	title = {Scalable and continuous access to pure cyclic polymers enabled by ‘quarantined’ heterogeneous catalysts},
	url = {https://m2.mtmt.hu/api/publication/33262683},
	author = {Yoon, Ki-Young and Noh, Jinkyung and Gan, Quan and Edwards, Julian P. and Tuba, Róbert and Choi, Tae-Lim and Grubbs, Robert H.},
	doi = {10.1038/s41557-022-01034-8},
	journal-iso = {NAT CHEM},
	journal = {NATURE CHEMISTRY},
	volume = {14},
	unique-id = {33262683},
	issn = {1755-4330},
	year = {2022},
	eissn = {1755-4349},
	pages = {1242-1248},
	orcid-numbers = {Yoon, Ki-Young/0000-0003-3257-6103; Noh, Jinkyung/0000-0002-9290-2321; Gan, Quan/0000-0001-5908-4163; Choi, Tae-Lim/0000-0001-9521-6450}
}

@article{MTMT:33062564,
	title = {Hydrolytic dehydrogenation of ammonia borane in neat water using recyclable zeolite-supported cyclic alkyl amino carbene (CAAC)–Ru catalysts},
	url = {https://m2.mtmt.hu/api/publication/33062564},
	author = {Balla, Áron and Nagyházi, Márton and Turczel, Gábor and Solt, Hanna Erzsébet and Rosenbergerné Mihályi, Magdolna and Hancsók, Jenő and Valyon, József and Nagy, Tibor and Kéki, Sándor and Anastas, Paul T. and Tuba, Róbert},
	doi = {10.1039/D2NJ03334H},
	journal-iso = {NEW J CHEM},
	journal = {NEW JOURNAL OF CHEMISTRY},
	volume = {46},
	unique-id = {33062564},
	issn = {1144-0546},
	abstract = {Highly effective ammonia borane dehydrogenation was carried out using a heterogenized ruthenium-CAAC complex in water.},
	year = {2022},
	eissn = {1369-9261},
	pages = {16309-16316},
	orcid-numbers = {Hancsók, Jenő/0000-0003-1959-7604; Valyon, József/0000-0002-3608-060X; Nagy, Tibor/0000-0001-8568-914X}
}

@article{MTMT:33014942,
	title = {Synthesis and catalytic olefin metathesis activity of amberlyst-15 supported cyclic and bicyclic alkyl amino carbene ruthenium complexes},
	url = {https://m2.mtmt.hu/api/publication/33014942},
	author = {Deme, János and Nagyházi, Márton and May, Zoltán and Hancsók, Jenő and Valyon, József and Kéki, Sándor and Tuba, Róbert and Turczel, Gábor},
	doi = {10.1007/s11144-022-02261-3},
	journal-iso = {REACT KINET MECH CATAL},
	journal = {REACTION KINETICS MECHANISMS AND CATALYSIS},
	volume = {135},
	unique-id = {33014942},
	issn = {1878-5190},
	abstract = {Amberlyst-15 supported cyclic alkyl amino carbene and bicyclic alkyl amino carbene ruthenium olefin metathesis catalysts for sustainable catalytic applications have been synthesized by the well-known wet impregnation method utilizing ionic complex/support interaction. Surface coverages are as high as 4 and 7 wt% were achieved in the case of the significantly higher pore volume Amberlyst-15, compared to Amberlyst-36. These phase separable catalysts show high activity in cross metathesis, ring closing metathesis and ethenolysis reactions compared to the reported heterogenized olefin metathesis catalysts. Leeching tests revealed no more than 1.5 ppm ruthenium content for the investigated metathesis reactions, which is well below the accepted 10 ppm limit in case of consumer products. © 2022, The Author(s).},
	year = {2022},
	eissn = {1878-5204},
	pages = {2519-2531},
	orcid-numbers = {Hancsók, Jenő/0000-0003-1959-7604; Valyon, József/0000-0002-3608-060X}
}

@article{MTMT:32853951,
	title = {Catalytic Decomposition of Long-Chain Olefins to Propylene via Isomerization-Metathesis Using Latent Bicyclic (Alkyl)(Amino)Carbene-Ruthenium Olefin Metathesis Catalysts},
	url = {https://m2.mtmt.hu/api/publication/32853951},
	author = {Nagyházi, Márton and Lukacs, Adam and Turczel, Gábor and Hancsók, Jenő and Valyon, József and Bényei, Attila Csaba and Kéki, Sándor and Tuba, Róbert},
	doi = {10.1002/anie.202204413},
	journal-iso = {ANGEW CHEM INT EDIT},
	journal = {ANGEWANDTE CHEMIE-INTERNATIONAL EDITION},
	volume = {61},
	unique-id = {32853951},
	issn = {1433-7851},
	abstract = {One of the most exciting scientific challenges today is the catalytic degradation of non-biodegradable polymers into value-added chemical feedstocks. The mild pyrolysis of polyolefins, including high-density polyethylene (HDPE), results in pyrolysis oils containing long-chain olefins as major products. In this paper, novel bicyclic (alkyl)(amino)carbene ruthenium (BICAAC-Ru) temperature-activated latent olefin metathesis catalysts, which can be used for catalytic decomposition of long-chain olefins to propylene are reported. These thermally stable catalysts show significantly higher selectivity to propylene at a reaction temperature of 75 degrees C compared to second generation Hoveyda-Grubbs or CAAC-Ru catalysts under ethenolysis conditions. The conversion of long-chain olefins (e.g., 1-octadecene or methyl oleate) to propylene via isomerization-metathesis is performed by using a (RuHCl)(CO)(PPh3)(3) isomerization co-catalyst. The reactions can be carried out at a BICAAC-Ru catalyst loading as low as 1 ppm at elevated reaction temperature (75 degrees C). The observed turnover number and turnover frequency are as high as 55 000 and 10 000 mol(propylene) mol(catalyst)(-1) h(-1), respectively.},
	keywords = {MECHANISM; ETHYLENE; Propylene; cracking; metathesis; propene; STABLE CARBENES; BEARING; RUTHENIUM COMPLEXES; 1-Butene; BICAAC; Hydrocarbon Decomposition; ISOMET},
	year = {2022},
	eissn = {1521-3773},
	orcid-numbers = {Hancsók, Jenő/0000-0003-1959-7604; Valyon, József/0000-0002-3608-060X}
}

@article{MTMT:32687686,
	title = {Synthesis and characterization of novel PEPPSI type bicyclic (alkyl)(amino)carbene (BICAAC)-Pd complexes},
	url = {https://m2.mtmt.hu/api/publication/32687686},
	author = {Nagyházi, Márton and Almási, Balázs and Lukács, Ádám and Bényei, Attila Csaba and Nagy, Tibor and Kéki, Sándor and Tuba, Róbert},
	doi = {10.1016/j.molstruc.2022.132483},
	journal-iso = {J MOL STRUCT},
	journal = {JOURNAL OF MOLECULAR STRUCTURE},
	volume = {1256},
	unique-id = {32687686},
	issn = {0022-2860},
	abstract = {A series of bicyclic alkylamino carbenes (BICAAC) (where N-aryl = dipp, mes, 2,6-dimethyl-4-(dimethylamino)phenyl, 5a–d) and their novel air- and moisture-resistant pyridine (pyridine, 4-dimethylaminopyridine) containing palladium Pd(II) complexes (6a–e) were synthetized and characterized. As novel examples of the PEPPSI (“pyridine enhanced precatalyst preparation stabilization and initiation”)-Pd compounds, the reported complexes have shown high activity in Mizoroki–Heck coupling reaction even at as low as 100 ppm loading (TON up to 10000). Kinetic studies revealed that reactions carried out in the presence of elemental mercury resulted decrease in activity. It indicates that the coupling reaction may have both molecular and Pd(0)-mediated catalytic paths. © 2022 The Authors},
	keywords = {PYRIDINE; Synthesis (chemical); Palladium compounds; carbenes; Mizoroki–Heck reaction; Mizoroki–Heck reaction; Synthesis and characterizations; Pd-PEPPSI; Precatalysts; 4-DIMETHYLAMINOPYRIDINE; PEPPSI complex; BICAAC; Palladium carbene complex; Bicyclic (alkyl)(amino)carbene; Palladium carbene complexes; Pd-“pyridine enhanced precatalyst preparation stabilization and initiation”; “pyridine enhanced precatalyst preparation stabilization and initiation” complex},
	year = {2022},
	eissn = {1872-8014},
	orcid-numbers = {Nagy, Tibor/0000-0001-8568-914X}
}

@article{MTMT:32219197,
	title = {Propylene synthesis via isomerization–metathesis of 1-hexene and FCC olefins},
	url = {https://m2.mtmt.hu/api/publication/32219197},
	author = {Novodárszki, Gyula and Szabó, Blanka and Auer, Róbert and Tóth, Katalin and Leveles, László and Barthos, Róbert and Turczel, Gábor and Pászti, Zoltán and Valyon, József and Rosenbergerné Mihályi, Magdolna and Tuba, Róbert},
	doi = {10.1039/D1CY00269D},
	journal-iso = {CATAL SCIENCE & TECHNOLOGY},
	journal = {CATALYSIS SCIENCE & TECHNOLOGY},
	volume = {11},
	unique-id = {32219197},
	issn = {2044-4753},
	year = {2021},
	eissn = {2044-4761},
	pages = {6257-6270},
	orcid-numbers = {Leveles, László/0000-0001-6097-2870; Valyon, József/0000-0002-3608-060X}
}