Results 171 to 180 of about 16,087 (218)
Some of the next articles are maybe not open access.

Pentacene‐Fused Diporphyrins

Chemistry – A European Journal, 2014
AbstractIn this work, we report the synthesis, spectroscopic characterization, and theoretical analysis of a linearly conjugated pentacene‐fused porphyrin dimer and cross‐conjugated quinone‐fused dinaphtho[2,3]porphyrins. These multichromophoric systems display non‐typical UV‐visible absorptions of either porphyrins or pentacenes/quinones.
Lin, Jiang   +6 more
openaire   +2 more sources

Ubiquitous Pentacene Monolayer on Metals Deposited onto Pentacene Films

Langmuir, 2007
Photoelectron spectroscopy (XPS and UPS) was used to study the deposition of metal layers (Ag, Cu, and Au) onto pentacene films. Very low work functions were measured (PhiAg = 3.91 eV, PhiCu = 3.93 eV, and PhiAu = 4.3 eV) for all of the metals, in agreement with results from the literature.
B, Jaeckel, J B, Sambur, B A, Parkinson
openaire   +2 more sources

PENTACENE AT HIGH PRESSURE

High Pressure Research, 2003
We report a high-pressure optical study of pentacene by Raman, absorption, and reflectance spectroscopy. Two modifications, denoted C and H, were used as starting material. Raman spectra indicate a sluggish phase transition of the polymorph C to the H-phase with a very low onset pressure of 0.2 GPa. The H-phase remains stable up to at least 11 GPa. The
Farina, L.   +5 more
openaire   +2 more sources

Robust, Soluble Pentacene Ethers

Organic Letters, 2004
We report the synthesis and characterization of a series of alkoxy-substituted silylethynylated pentacene derivatives (R = CH(2)CH(2), CHCH, CH(2)). All three compounds are easily prepared, soluble in common organic solvents, and stable both as solids and in solution.
Marcia M, Payne   +3 more
openaire   +2 more sources

Stabilizing Pentacene By Cyclopentannulation

Angewandte Chemie International Edition, 2015
AbstractA new class of stabilized pentacene derivatives with externally fused five‐membered rings are prepared by means of a key palladium‐catalyzed cyclopentannulation step. The target compounds are synthesized by chemical manipulation of a partially saturated 6,13‐dibromopentacene precursor that can be fully aromatized in a final step through a DDQ ...
Sambasiva R, Bheemireddy   +6 more
openaire   +2 more sources

Pentacene based Onsager crosses

Chemical Communications, 2016
A dearomatization/aromatization strategy accesses two pentacene based molecular caltrops with improved solubility and film forming properties.
F L, Geyer   +6 more
openaire   +2 more sources

Exploring Electronically Polarized Pentacenes

Organic Letters, 2008
Unsymmetrically functionalized pentacenes with electron-rich and/or -poor substituents at the 6- and 13-positions were synthesized. The electronic influence was evaluated by solution-state UV-vis absorption and emission spectroscopies. These materials exhibit good solubility in common organic solvents and are stable in the presence of air and water.
Dan, Lehnherr   +2 more
openaire   +2 more sources

Pentacene Films on Cu(119)

Langmuir, 2010
The molecular structure of thin pentacene film grown on a Cu(119) surface has been studied by near-edge X-ray absorption fine structure spectroscopy and scanning tunneling microscopy. The interaction between the π-molecular orbitals delocalized on the aromatic rings and the underlying copper substrate was deduced from XAS spectra.
Annese E, Vobornik I, Rossi G, Fujii J
openaire   +3 more sources

Water soluble pentacene

Journal of Materials Chemistry C, 2013
A water soluble pentacene, potassium 3,3′-(pentacene-6,13-diylbis(sulfanediyl))dipropanoate (4), has been synthesized and characterized. The synthesis of 4 is straightforward and scalable, and its isolation does not require time consuming chromatographic separations.
Chandrani Pramanik   +9 more
openaire   +1 more source

Pentacene and poly-pentacene as graphene nanoribbons

Solid State Communications, 2014
Abstract The development of electronic devices based on the unique electronic properties of graphene requires the large scale synthesis of graphene nanoribbons which remains a significant challenge. A possible way around this is to seek existing molecules that can be readily chemically synthesized and have the structure of graphene nano-ribbons.
openaire   +1 more source

Home - About - Disclaimer - Privacy