Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ronald B. M. Ansems"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 956-968 (2014)
Circumtrindene (6, C36H12), one of the largest open geodesic polyarenes ever reported, exhibits fullerene-like reactivity at its interior carbon atoms, whereas its edge carbons react like those of planar polycyclic aromatic hydrocarbons (PAHs). The B
Externí odkaz:
https://doaj.org/article/9b8fd07c62bf4cd6a1bed594b45baf9b
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 956-968 (2014)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Circumtrindene (6, C36H12), one of the largest open geodesic polyarenes ever reported, exhibits fullerene-like reactivity at its interior carbon atoms, whereas its edge carbons react like those of planar polycyclic aromatic hydrocarbons (PAHs). The B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1387d439e57736d468f8bef13c37e33c
https://doaj.org/article/9b8fd07c62bf4cd6a1bed594b45baf9b
https://doaj.org/article/9b8fd07c62bf4cd6a1bed594b45baf9b
Autor:
Ronald B. M. Ansems, Lawrence T. Scott
Publikováno v:
Journal of Physical Organic Chemistry. 17:819-823
Circumtrindene (1), a C36H12 geodesic polyarene that represents 60% of fullerene-C60, forms cation–π complexes with both silver ion (1·Ag+) and tetramethylammonium ion [(Me)4N+·1] in chloroform solution at room temperature (Ka>20 M−1 for both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56800a6b1afef4fb80cc3ebcc10ff51c
https://doi.org/10.1002/poc.800
https://doi.org/10.1002/poc.800
Publikováno v:
Journal of the American Chemical Society. 122:2719-2724
The title compound (1), which had previously been available in only 0.2% yield by flash vacuum pyrolysis (FVP) of decacyclene (2) at 1200−1300 °C, has now been prepared in 25−27% yield by FVP of 3,9,15-trichlorodecacyclene (5b) at 1100 °C. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ef297e409c1131cb0788c8b16e02efe
https://doi.org/10.1021/ja993028n
https://doi.org/10.1021/ja993028n
Autor:
Lawrence T. Scott, Stefan Hagen, Ronald B. M. Ansems, Matthew S. Bratcher, Hindy E. Bronstein, Dorin V. Preda
Publikováno v:
Pure and Applied Chemistry. 71:209-219
Polycyclic aromatic hydrocarbons (PAHs) in which five-membered rings have been interspersed among the six-membered rings generally display curved p systems that can be either fully closed (fullerenes) or partially open (bowl-shaped fullerene fragment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6ce20d3c567d596da6f549988655fb
https://doi.org/10.1351/pac199971020209
https://doi.org/10.1351/pac199971020209
Autor:
Matthew S. Bratcher, Lawrence T. Scott, Ronald B. M. Ansems, Hindy E. Bronstein, Stefan Hagen, Dorin V. Preda
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00ae8ca9687dd9faa4b2ae8b53720ec8
https://doi.org/10.1002/chin.199952267
https://doi.org/10.1002/chin.199952267
Autor:
Matthew S. Bratcher, Dorin V. Preda, Stefan Hagen, Ronald B. M. Ansems, Lawrence T. Scott, Hindy E. Bronstein
Publikováno v:
ChemInform. 31
Polycyclic aromatic hydrocarbons (PAHs) in which five-membered rings have been interspersed among the six-membered rings generally display curved p systems that can be either fully closed (fullerenes) or partially open (bowl-shaped fullerene fragment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3500b41de7f1994c765a28adfc7ac9a2
https://doi.org/10.1002/chin.200002272
https://doi.org/10.1002/chin.200002272