Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Mark R. Mason"'
Publikováno v:
Journal of Organometallic Chemistry. 984:122554
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44eca2c12e820db2b1e248e73d974822
https://doi.org/10.1016/j.jorganchem.2022.122554
https://doi.org/10.1016/j.jorganchem.2022.122554
Autor:
Mark R. Mason
Publikováno v:
Physical Sciences Reviews. 5
This paper provides a brief overview of the formation, organization, and mission of the School of Green Chemistry and Engineering (SGCE) at the University of Toledo, and a description of SGCE efforts to introduce principles of green chemistry and gre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3175a5d4b3595eebf4cdaf5be8245473
https://doi.org/10.1515/psr-2020-0005
https://doi.org/10.1515/psr-2020-0005
Publikováno v:
Journal of Organometallic Chemistry. 944:121830
Acid-catalyzed condensation of fluorenylacetaldehyde diethylacetal (1) or indenylacetaldehyde diethylacetal (2) with 3-methylindole yields fluorenylbis(3-methylindolyl)ethane (3) or indenylbis(3-methylindolyl)ethane (4), respectively. Compounds 3 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::072ab95e3f38e92080e02836f3e64abb
https://doi.org/10.1016/j.jorganchem.2021.121830
https://doi.org/10.1016/j.jorganchem.2021.121830
Autor:
Yihong Zhao, Kristin Kirschbaum, Li Jia, Mark R. Mason, Christopher G. Gianopoulos, Nishant Kumar
Publikováno v:
Dalton Transactions. 45:13787-13797
Aluminum halide, alkoxide and amide complexes 2-6 of the form (N,N)AlX2-nYn (n = 0, 1 and (N,N) = 1,9-dimesityl-5-phenyldipyrromethene (1)) were synthesized and characterized by NMR spectroscopy and X-ray crystallography. The in situ generated lithiu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2ade5973e75d8cb03677383c1cf6bf4
https://doi.org/10.1039/c6dt02449a
https://doi.org/10.1039/c6dt02449a
Publikováno v:
Organometallics. 33:4503-4511
Reactions of an appropriate organoaluminum reagent with a sterically demanding dipyrromethene (2) produced the monomeric complexes (N,N)AlR2 (where (N,N) is deprotonated dipyrromethene; R = Me (3),...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c50743c365503de588a11d0e05cd95dd
https://doi.org/10.1021/om500730g
https://doi.org/10.1021/om500730g
Publikováno v:
Synlett. 25:977-982
Gramine-based N-substituted phosphines were synthesized and utilized as ligands in Suzuki–Miyaura coupling of aryl bromides and chlorides in the room temperature ionic liquid trihexyltetradecylphosphonium bis(trifluoromethanesulfonyl)imide. Increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abc3dcf7d7585d09fe7d8968d0ee5485
https://doi.org/10.1055/s-0033-1340846
https://doi.org/10.1055/s-0033-1340846
Publikováno v:
Organometallics. 31:191-196
Reactions of tris(3-methylindolyl)methane, bis(3-methylindolyl)-2-methoxyphenylmethane, and bis(3-methylindolyl)phenylmethane with THF·BH3 result in hydrogen elimination and yield the corresponding boron monohydride complexes (3-CH3C8H4NH)HC(3-CH3C8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d992d6ea03a86e4dabc51dac2a28af83
https://doi.org/10.1021/om2006694
https://doi.org/10.1021/om2006694
Publikováno v:
Organometallics. 29:5927-5935
Reactions of 3-methylindole with one equivalent of R3Al produce the N-indolide-bridged dimers [(3-CH3C8H5N)AlR2]2 (R = Me (3a), Et (3b), iBu (3c)). NMR spectroscopy (1H, 13C) demonstrates that compounds 3a, 3b, and 3c each exist in solution as a mixt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c5b290a3767804692bd7cd14b50c25c
https://doi.org/10.1021/om100781k
https://doi.org/10.1021/om100781k
Autor:
Mark R. Mason
Publikováno v:
Encyclopedia of Inorganic and Bioinorganic Chemistry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::191f935d32990fe659054627768486d1
https://doi.org/10.1002/9781119951438.eibc2333
https://doi.org/10.1002/9781119951438.eibc2333
