نتایج جستجو برای: naphthalenes

تعداد نتایج: 1445  

2011
Kew-Yu Chen Ming-Jen Chang Tzu-Chien Fang

The title compound, C(15)H(12)Br(2), comprises a norbornane unit having a dibromo-naphthalene ring fused on one side. Both Br atoms are twisted slightly out of the plane of the naphthalene ring system with a Br-C-C-Br torsion angle of 5.3 (5)°. In the crystal, mol-ecules are linked by weak inter-molecular C-H⋯Br hydrogen bonds, forming an infinite C(9) chain along [110].

Journal: :Chemical communications 2011
Anindita Das Suhrit Ghosh

An effective supramolecular strategy for self-sorting between naphthalene-diimide (NDI) acceptor and dialkoxy-naphthalene (DAN) donor organogelators is reported. The concept is based on mismatch in the placement of the two amide functionalities in the donor and acceptor chromophores so that self-sorting ensured maximum effect of H-bonding.

Journal: :Journal of the American Chemical Society 2009
Jorge García-Fortanet Florian Kessler Stephen L Buchwald

An intramolecular enantioselective metal-catalyzed dearomatization reaction is described. This procedure allows the dearomatization of naphthalene derivatives through an electrophilic aromatic substitution-type reaction on a Pd(II) intermediate. The high yields and enantioselectivities achieved make this procedure a valuable method for synthetic chemists.

2011
Hoong-Kun Fun Ching Kheng Quah B. Narayana Prakash S. Nayak B. K. Sarojini

In the title compound, C(18)H(14)BrNO, the naphthalene ring system and the benzene ring form dihedral angles of 78.8 (2) and 19.7 (2)°, respectively, with the acetamide C-C(=O)-N plane. The naphthalene ring system forms a dihedral angle of 64.88 (19)° with the benzene ring. In the crystal, mol-ecules are linked via inter-molecular bifurcated (N,C)-H⋯O hydrogen bonds, generating an R(2) (1)(6) r...

Journal: :Organic letters 2011
Tridib Sarma Pradeepta K Panda P T Anusha S Venugopal Rao

Naphthobipyrrole-derived porphycenes are synthesized for the first time via McMurry coupling of the β-alkylated 2,9-diformylnaphthobipyrrole derivatives, which in turn were prepared easily from 2,3-naphthalene bishydrazine in four steps. Insertion of nickel into the porphycene core results in transformation of the rectangular N4-core into a square type geometry owing to the fusion of naphthalen...

Journal: :Physical chemistry chemical physics : PCCP 2013
D Fazzi F Scotognella A Milani D Brida C Manzoni E Cinquanta M Devetta L Ravagnan P Milani F Cataldo L Lüer R Wannemacher J Cabanillas-Gonzalez M Negro S Stagira C Vozzi

The dynamics of excited states in α,ω-dinaphthylpolyyne, a class of linear sp-carbon chains, has been investigated by ultrafast transient absorption spectroscopy and DFT//TDDFT calculations. We show that the role of molecular conformers, in which end-capped naphthalene rings are planar or perpendicular to the polyyne plane, is fundamental for understanding both the steady state properties, such...

2008
Conrad Fischer Tobias Gruber Wilhelm Seichter Edwin Weber Bakhtiyar T. Ibragimov

The molecule of the title compound, C(24)H(36)N(2)O(2)S, displays a U-shaped conformation. The prominent inter-molecular inter-actions are N-H⋯O hydrogen bonds, resulting in the formation of dimers. Additional C-H⋯π contacts involving one of the methyl-ene groups of the macrocycle and the naphthalene rings of a neighbouring mol-ecule stabilize the packing structure. In the crystal structure, th...

2004
Sebastian A. Kaiser Marshall B. Long

In planar laser-induced fluorescence (PLIF), naphthalenes are commonly used as tracers for diesel-like fuels and fuel surrogates. Previously, such a technique was used to visualize the air–fuel mixing in a mesoscale ( 10 cm device volume) burner prototype running on dodecane as a single-component JP-8 surrogate. For quantification of this technique, the influence of temperature, oxygen quenchin...

Journal: :Molecules 2015
James Tancock Thomas Wirth

New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement products.

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