نتایج جستجو برای: naphthalenes

تعداد نتایج: 1445  

2013
Danuta Bauman Thomas Hanemann Eryk Wolarz

für Naturforschung in cooperation with the Max Planck Society for the Advancement of Science under a Creative Commons Attribution 4.0 International License. Dieses Werk wurde im Jahr 2013 vom Verlag Zeitschrift für Naturforschung in Zusammenarbeit mit der Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. digitalisiert und unter folgender Lizenz veröffentlicht: Creative Commons Namen...

2013
Jae Kyun Lee Kee Dal Nam Joo Hwan Cha Yong Seo Cho Joon Kyun Lee

The title compound, C25H19N, adopts an E conformation about the C=N bond. The naphthalene ring system and the phenyl rings form dihedral angles 38.1 (1), 46.9 (8) and 48.5 (1)°, respectively, with the mean plane of the central enimino fragment. The crystal packing exhibits no directional close contacts.

2013
Takehiro Tsumuki Ryo Takeuchi Hiroyuki Kawano Noriyuki Yonezawa Akiko Okamoto

In the title compound, C36H28O4, the 1-naphthoyl groups at the 1- and 8-positions of the central 2,7-dieth-oxy-naphthalene ring system are aligned almost anti-parallel and make a dihedral angle of 76.59 (4)°. The dihedral angles between the central 2,7-dieth-oxy-naphthalene ring system and the terminal naphthalene ring systems are 86.48 (4) and 83.97 (4)°. In the crystal, C-H⋯π inter-actions be...

2011
S. Selvanayagam K. Ravikumar P. Saravanan R. Raghunathan

In the title compound, C(32)H(28)N(2)O(2), the pyrrolidine ring adopts an envelope conformation, whereas the cyclo-hexa-none ring in the tetra-hydro-naphthalene fused-ring system adopts a half-chair conformation. The oxindole ring system is oriented at an angle of 48.2 (1)° with respect to the naphthyl ring system. An intra-molecular C-H⋯O close contact is observed. In the crystal, mol-ecules a...

Journal: :Chemical communications 2015
Diego Rodríguez-Lojo Dolores Pérez Diego Peña Enrique Guitián

Phenyl-substituted tetra-, penta-, hexa- and octacenes were easily obtained starting from a readily available naphthalene-based bisaryne precursor. This approach to large acenes involves a sequence of two Diels-Alder cycloadditions with dienones followed by two CO extrusion reactions.

2011
Xiao-Guang Bai Hong-Tao Liu Yu-Cheng Wang Ju-Xian Wang

In the cation of the title compound, C(18)H(20)ClN(4)O(3)S(+)·Cl(-), the tetra-hydro-pyridinium ring assumes a half-chair conformation. The dihedral angle between the pyrazole ring and the naphthalene ring system is 75.19 (6)°. In the crystal, ions are linked into a three-dimensional network by N-H⋯O, N-H⋯Cl and O-H⋯Cl hydrogen bonds and weak π-π stacking inter-actions with centroid-centroid di...

2013
Mark L. Wolfenden Raj K. Dhar Frank R. Fronczek Steven F. Watkins

The title compound, C(26)H(18), consists of a benzene ring with meta-substituted 2-naphthalene substituents, which are essentially planar [r.m.s. deviations = 0.022 (1) and 0.003 (1) Å]. The conformation is syn, with equivalent torsion angles about the benzene-naphthalene bonds of -36.04 (13) and +34.14 (13)°. The mol-ecule has quasi-C(s) mol-ecular symmetry.

Journal: :Chemical communications 2010
Sergio J Garibay Seth M Cohen

Amino, bromo, nitro, and naphthalene functionalized UiO-66 metal-organic frameworks have been synthesized through reticular chemistry. UiO-66-NH(2) is shown to be suitable for postsynthetic modification with a variety of anhydrides to generate new, functionalized frameworks.

Journal: :Physical chemistry chemical physics : PCCP 2014
Mei-Yu Yeh Hsin-Chieh Lin

Supramolecular assembly of donor-acceptor complexes as the key component in organic functional nanomaterials is a promising approach for future electronic devices. One representative example of the donor-acceptor complexes is the naphthalene diimide-pyrene (NDI-Py) system, which shows fascinating photoelectric properties. Herein, the analysis of the π-π interactions between NDI and Py has been ...

Journal: :Chemical communications 2015
F Doria A Oppi F Manoli S Botti N Kandoth V Grande I Manet M Freccero

A non-fluorescent naphthalene diimide (NDI) dimer, conjugating red and blue NDI dyes, becomes red/NIR emitting upon G-quadruplex binding. The fluorescence lifetime which is significantly different for the complexes, the G-quadruplex/dimer and the weakly emitting ds-DNA/dimer is the key feature for the development of new rationally engineered G-quadruplex sensors.

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