Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Zachary W. Schroeder"'
Autor:
Zachary W. Schroeder, Robert McDonald, Michael J. Ferguson, Wesley A. Chalifoux, Rik R. Tykwinski, Dan Lehnherr
Publikováno v:
The Journal of Organic Chemistry. 87:16236-16249
We report a general method for the desymmetrization of 6,13-pentacenequinone to access ethynylated pentacene ketones, namely, 13-hydroxy-13-(ethynylated)pentacene-6(13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c191e9f821a013460573213d5aceefdd
https://doi.org/10.1021/acs.joc.2c01755
https://doi.org/10.1021/acs.joc.2c01755
Publikováno v:
RSC Advances. 11:39564-39569
Nickel-mediated Yamamoto coupling provides a concise and efficient synthesis of triphenylene derivatives, including electron-deficient discotic mesogens.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d80e4a180130f41c80ac8a26f2073d56
https://doi.org/10.1039/d1ra07931j
https://doi.org/10.1039/d1ra07931j
Autor:
Louise N. Dawe, Lana K. Hiscock, Christina Rodriguez, Rachel Kiriakopoulos, Zachary W. Schroeder
Publikováno v:
Canadian Journal of Chemistry. 98:273-277
Crystal engineered organic frameworks assembled using hydrogen bonding are known, and examples constructed from hydroxypyridine/pyridone as the dominant source of hydrogen bonding have been reported. Less explored are analogous systems based on malei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b02171ca9c3ccd2b92a2edeb5758439
https://doi.org/10.1139/cjc-2019-0474
https://doi.org/10.1139/cjc-2019-0474
Autor:
Barbora Balónová, Kenneth E. Maly, Marta Tomas Piqueras, Delara Joekar, Barry A. Blight, Victoria Jarvis, Zachary W. Schroeder, Louise N. Dawe, Lana K. Hiscock
Publikováno v:
Inorganic Chemistry. 58:16317-16321
The synthesis of the asymmetric ligand 3-phenyl-1-(pyridin-2-yl)-1H-pyrazol-5-amine (L1) and its single-crystal X-ray structure are reported. L1 displays crystallographic symmetry (orthorhombic, Pccn) higher than its molecular symmetry (point group C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::133bba97b8f45e79dcf18f81ccbd6ac8
https://doi.org/10.1021/acs.inorgchem.9b02765
https://doi.org/10.1021/acs.inorgchem.9b02765
Autor:
Rasmus Ringström, Fredrik Edhborg, Zachary W. Schroeder, Lan Chen, Michael J. Ferguson, Rik R. Tykwinski, Bo Albinsson
Publikováno v:
Chemical science. 13(17)
Three pentacene dimers have been synthesized to investigate the effect of molecular rotation and rotational conformations on singlet fission (SF). In all three dimers, the pentacene units are linked by a 1,4-diethynylphenylene spacer that provides al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa1e9a62459690b7084c129344504618
https://pubmed.ncbi.nlm.nih.gov/35655894
https://pubmed.ncbi.nlm.nih.gov/35655894
Publikováno v:
RSC advances. 11(62)
Substituted triphenylenes show promise as organic semiconductors because of their ability to form columnar liquid crystalline phases featuring extended π-stacked arrays. While there are several methods for preparing triphenylenes, including oxidativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dda14d16b921934292f44dcd00a22c7e
https://pubmed.ncbi.nlm.nih.gov/35492499
https://pubmed.ncbi.nlm.nih.gov/35492499
Autor:
Lana K, Hiscock, Delara, Joekar, Barbora, Balonova, Marta, Tomas Piqueras, Zachary W, Schroeder, Victoria, Jarvis, Kenneth E, Maly, Barry A, Blight, Louise N, Dawe
Publikováno v:
Inorganic chemistry. 58(24)
The synthesis of the asymmetric ligand 3-phenyl-1-(pyridin-2-yl)-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::594b1c91aa113de9c907ad0936cca4c8
https://pubmed.ncbi.nlm.nih.gov/31799844
https://pubmed.ncbi.nlm.nih.gov/31799844
Publikováno v:
European Journal of Inorganic Chemistry. 2018:167-172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1bc6305c4f1d8ffb5e636566625b57d
https://doi.org/10.1002/ejic.201701220
https://doi.org/10.1002/ejic.201701220
Autor:
Lana K. Hiscock, Delara Joekar, Zachary W. Schroeder, Victoria Jarvis, Kenneth E. Maly, Louise Dawe
The synthesis and single crystal structures of 3-phenyl-1-(pyridin-2-yl)-1H-pyrazol-5-amine (L1) and its complex with ZnCl2 are reported. L1 exhibits supercooling, with a difference in melting and solidification points of over 100 oC. The complex [L1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe0c7d30cb914736fa69d9cd522ddde
https://doi.org/10.26434/chemrxiv.10078943
https://doi.org/10.26434/chemrxiv.10078943
Publikováno v:
Acta crystallographica. Section C, Structural chemistry. 73(Pt 11)
Benzothiazole derivatives are a class of privileged molecules due to their biological activity and pharmaceutical applications. One route to these molecules is via intramolecular cyclization of thioureas to form substituted 2-aminobenzothiazoles, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8519f010692563eae9b77d0bc8c1b83c
https://pubmed.ncbi.nlm.nih.gov/29111517
https://pubmed.ncbi.nlm.nih.gov/29111517