Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Anna CHROSTOWSKA"'
Autor:
Ziyong Wang, Chen Zhang, Jason Wu, Bo Li, Anna Chrostowska, Panaghiotis Karamanis, Shih-Yuan Liu
Publikováno v:
Journal of the American Chemical Society. 145:5624-5630
Autor:
Yuanzhe Zhang, Ziyong Wang, Walid Lamine, Senmiao Xu, Bo Li, Anna Chrostowska, Karinne Miqueu, Shih-Yuan Liu
The reaction mechanism of the Pd/Senphos-catalyzed trans-hydroboration reaction of 1,3- enynes was investigated using various experimental techniques, including deuterium and double cross-over labeling experiments, X-ray crystallographic characteriza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9b097572f155c36377ebd4376a4eb5
https://doi.org/10.26434/chemrxiv-2022-cmzdf
https://doi.org/10.26434/chemrxiv-2022-cmzdf
Publikováno v:
Chemical Physics Letters. :140615
Autor:
Rongala Ramalakshmi, Anna Chrostowska, Clovis Darrigan, Shih-Yuan Liu, Bo Li, Kiran Sagar Unikela, Min Chen
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2021, 60 (3), pp.1556-1560. ⟨10.1002/anie.202010556⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2021, 60 (3), pp.1556-1560. ⟨10.1002/anie.202010556⟩
International audience; The first example of a BN-doped cycloparaphenylene BN-[10]CPP was synthesized and characterized. Its reactivity and photophysical properties were evaluated in direct comparison to its carbonaceous analogues Mes-[10]CPP and [10
Publikováno v:
New Journal of Chemistry
New Journal of Chemistry, Royal Society of Chemistry, 2021, 45 (48), pp.22876-22887. ⟨10.1039/d1nj05137g⟩
New Journal of Chemistry, Royal Society of Chemistry, 2021, 45 (48), pp.22876-22887. ⟨10.1039/d1nj05137g⟩
International audience; A series of C(10)-substituted derivatives of 2-Ph-3H-[1,2,4]triazino[5,6,1-kl]phenoxazin-3-yl was obtained using the aza-Pschorr, photochemical and radical-induced cyclization reactions, and through functional group transforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c00fa7af8b32a05100b3699e30a05d89
https://hal-univ-pau.archives-ouvertes.fr/hal-03508968
https://hal-univ-pau.archives-ouvertes.fr/hal-03508968
Autor:
Jean-Marc Sotiropoulos, Karinne Miqueu, Bo Li, Anna Chrostowska, Ziyong Wang, Jason Wu, Walid Lamine, Shih-Yuan Liu
Publikováno v:
Angew Chem Int Ed Engl
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2021, 60 (39), pp.21231-21236. ⟨10.1002/anie.202108534⟩
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2021, 60 (39), pp.21231-21236. ⟨10.1002/anie.202108534⟩
International audience; A new family of carbon-bound boron enolates, generated by a kinetically controlled halogen exchange between chlorocatecholborane and silylketene acetals, is described. These C−boron enolates are demonstrated to activate 1,3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd3901200d7c03975af480017c6d993
https://europepmc.org/articles/PMC8440383/
https://europepmc.org/articles/PMC8440383/
Publikováno v:
Journal of Physical Chemistry A
Journal of Physical Chemistry A, American Chemical Society, 2019, 123 (28), pp.6003-6015. ⟨10.1021/acs.jpca.9b04266⟩
Journal of Physical Chemistry A, 2019, 123 (28), pp.6003-6015. ⟨10.1021/acs.jpca.9b04266⟩
Journal of Physical Chemistry A, American Chemical Society, 2019, 123 (28), pp.6003-6015. ⟨10.1021/acs.jpca.9b04266⟩
Journal of Physical Chemistry A, 2019, 123 (28), pp.6003-6015. ⟨10.1021/acs.jpca.9b04266⟩
International audience; Hydrazine-boranes (HNNH·BH and HB·NHNH·BH) have been proposed for the storage of hydrogen, but these compounds have not created scope for extensive research works as ammonia- and methylamine-boranes have made these last dec
Publikováno v:
Journal of Physical Chemistry A
Journal of Physical Chemistry A, American Chemical Society, 2020, 124, pp.9777-9782. ⟨10.1021/acs.jpca.0c07900⟩
Journal of Physical Chemistry A, American Chemical Society, 2020, 124 (47), pp.9777-9782. ⟨10.1021/acs.jpca.0c07900⟩
Journal of Physical Chemistry A, American Chemical Society, 2020, 124, pp.9777-9782. ⟨10.1021/acs.jpca.0c07900⟩
Journal of Physical Chemistry A, American Chemical Society, 2020, 124 (47), pp.9777-9782. ⟨10.1021/acs.jpca.0c07900⟩
International audience; Fusion of benzene, naphthalene, and phenalene rings with the D ring of the planar Blatter radical leads to extension of the π-system and increased spin delocalization. The effect of this π-extension and the position of the r
Autor:
Clovis Darrigan, Paulina Bartos, Anna Pietrzak, Aniket A. Hande, Piotr Kaszynski, Patrick Baylère, Anna Chrostowska
Publikováno v:
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2020, 22 (41), pp.23637-23644. ⟨10.1039/D0CP03896B⟩
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2020, 22 (41), pp.23637-23644. ⟨10.1039/d0cp03896b⟩
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2020, 22 (41), pp.23637-23644. ⟨10.1039/D0CP03896B⟩
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2020, 22 (41), pp.23637-23644. ⟨10.1039/d0cp03896b⟩
International audience; The electronic structure of Blatter radicals and a series of C(10)-substituted derivatives of 2-phenyl-3H-[1,2,4]triazino[5,6,1-kl]phenoxazin-3-yl (planar Blatter radicals) containing H, F, Cl, Br, CN, CF3 and OMe substituents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf97b5b0031c8123447087a4ee6627ea
https://hal-univ-pau.archives-ouvertes.fr/hal-03025384
https://hal-univ-pau.archives-ouvertes.fr/hal-03025384
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2020, 56 (26), pp.3749-3752. ⟨10.1039/D0CC00869A⟩
Chem Commun (Camb)
Chemical Communications, Royal Society of Chemistry, 2020, 56 (26), pp.3749-3752. ⟨10.1039/D0CC00869A⟩
Chem Commun (Camb)
International audience; A BN indole-containing aromatic scaffold has been synthesized and the cation–π binding ability characterized by nuclear magnetic resonance (NMR) monitored titrations. The resulting chemical shifts were analyzed using a non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::056f74015f1efa00ffd2fe914eb67482
https://hal.archives-ouvertes.fr/hal-02499864
https://hal.archives-ouvertes.fr/hal-02499864