Search results for "Benzene"
showing 10 items of 1701 documents
CCDC 1508753: Experimental Crystal Structure Determination
2016
Related Article: Juanzhu Yan, Haifeng Su, Huayan Yang, Chengyi Hu, Sami Malola, Shuichao Lin, Boon K. Teo, Hannu Häkkinen, and Nanfeng Zheng|2016|J.Am.Chem.Soc.|138|12751|doi:10.1021/jacs.6b08100
CCDC 1858306: Experimental Crystal Structure Determination
2018
Related Article: A.J. Peloquin, M.B. Smith, B.J. O'Connell, K.B. Ghiassi, G.J. Balaich, S.T. Iacono|2018|Acta Crystallogr.,Sect.E:Cryst.Commun.|74|1190|doi:10.1107/S2056989018010794
CCDC 1873283: Experimental Crystal Structure Determination
2018
Related Article: Maciej Bujak, Hans-Georg Stammler, Sebastian Blomeyer, Norbert W. Mitzel|2019|Chem.Commun.|55|175|doi:10.1039/C8CC08980A
CCDC 658149: Experimental Crystal Structure Determination
2008
Related Article: D.Schollmeyer, O.V.Shishkin, T.Ruhl, M.O.Vysotsky|2008|CrystEngComm|10|715|doi:10.1039/b716442d
CCDC 1886744: Experimental Crystal Structure Determination
2019
Related Article: Marco Saccone, Michael Pfletscher, Sven Kather, Christoph Wölper, Constantin Daniliuc, Markus Mezger, Michael Giese|2019|J.Mater.Chem.C|7|8643|doi:10.1039/C9TC02787D
CCDC 644919: Experimental Crystal Structure Determination
2008
Related Article: F.Durola, L.Russo, J.-P.Sauvage, K.Rissanen, O.S.Wenger|2007|Chem.-Eur.J.|13|8749|doi:10.1002/chem.200700684
CCDC 1828644: Experimental Crystal Structure Determination
2018
Related Article: Joaquín Viqueira, María L. Durán, José A. García-Vázquez, Jesús Castro, Carlos Platas-Iglesias, David Esteban-Gómez, Gloria Alzuet-Piña, Angeles Moldes, Otaciro R. Nascimento|2018|New J.Chem.|42|15170|doi:10.1039/C8NJ03292K
Spin Trapping of Carbon-Centered Ferrocenyl Radicals with Nitrosobenzene
2015
In contrast to metal centered 17 valence electron radicals, such as [Mn(CO)5]•, ferrocenium ions [Fe(C5H5)2]+ (1+), [Fe(C5Me5)2]+ (2+), [Fe(C5H5)(C5H4Et)]+ (3+), [Fe(C5H5)(C5H4NHC(O)Me)]+ (4+), and [Fe(C5H5)(C5H4NHC(S)Me)]+ (5+) do not add to nitrosobenzene PhNO to give metal-coordinated stable nitroxyl radicals. In the presence of the strong and oxidatively stable phosphazene base tert-butylimino-tris(dimethylamino)phosphorane, the quite acidic ferrocenium ions 1+–5+ are deprotonated to give a pool of transient and persistent radicals with different deprotonation sites [1–Hx]•–[5–Hx]•. One rather persistent iron-centered radical [4–HN]•, deprotonated at the nitrogen atom, has been detected…
Reactive surface coatings based on polysilsesquioxanes: universal method toward light-responsive surfaces.
2011
Reactive surface coatings were used as an ideal precursor coating for the fabrication of three different photoswitchable surface coatings in parallel. Different light-responsive moieties, such as azobenzene, salicylideneaniline, and spiropyran, were immobilized on glass, polycarbonate, and steel surfaces. Independent from the underlying substrate, wettability could be switched reversibly by UV irradiation. The maximum switching range was obtained after functionalization of the reactive coating with spiropyran, resulting in a contact angle difference between the two isomeric states of almost 30°.
Nitramino, NRNO2 (R = H, CH3), as a substituent.13C and15N NMR spectroscopic study of nitraminobenzenes and -pyridines
1993
In order to clarify the special properties of the aryl-bound nitramino substituent NRNO 2 (R=H, CH 3 ), 13 C and 15 N NMR spectra of six nitraminobenzenes and nine nitraminopyridines were measured in DMSO-d 6 and their chemical shifts assigned. 1 H NMr chemical shifts and spin-spin coupling constants of all the compounds were also determined. In contrast to the behaviour of nitropyridines or -benzenes studied previously, most of the present compounds gave very broad 17 O NMR lines even at elevated temperatures and their 17 O NMR data were not useful for any reliable conclusions