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Search for "semiconductor" in Full Text gives 78 result(s) in Beilstein Journal of Organic Chemistry.

Separation and identification of indene–C70 bisadduct isomers

  • Bolong Zhang,
  • Jegadesan Subbiah,
  • David J. Jones and
  • Wallace W. H. Wong

Beilstein J. Org. Chem. 2016, 12, 903–911, doi:10.3762/bjoc.12.88

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  • separation; electron acceptor; fullerene bisadduct; organic solar cell; regioisomers; Introduction Organic solar cells (OSCs) are an emerging renewable energy technology that has achieved remarkable progress over the past two decades. Compared to traditional inorganic semiconductor solar cells, OSCs promise
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Published 06 May 2016

Syntheses of dibenzo[d,d']benzo[2,1-b:3,4-b']difuran derivatives and their application to organic field-effect transistors

  • Minh Anh Truong and
  • Koji Nakano

Beilstein J. Org. Chem. 2016, 12, 805–812, doi:10.3762/bjoc.12.79

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  • . Keywords: furan; heteroacenes; organic field-effect transistors; organic semiconductor; Introduction Organic semiconductors have significantly been developed in the past two decades by virtue of their advantages, such as low weight, flexibility, large-area processability, which are different features from
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Published 26 Apr 2016

Creating molecular macrocycles for anion recognition

  • Amar H. Flood

Beilstein J. Org. Chem. 2016, 12, 611–627, doi:10.3762/bjoc.12.60

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  • design. The long-term ramifications include the ability to create semiconductor structures by simple self-assembly. Thus, the goal is to contribute scientific understanding on how to program the nanostructures of advanced technology by employing bottom-up molecular design. The design and building of a
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Published 31 Mar 2016

Bright molecules for sensing, computing and imaging: a tale of two once-troubled cities

  • A. Prasanna de Silva

Beilstein J. Org. Chem. 2015, 11, 2774–2784, doi:10.3762/bjoc.11.298

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  • identification so that they can be tracked as they go through the processes of discovery and evaluation. However these beads are too small to be tagged by semiconductor-based radiofrequency identification (RFID) chips [66], which would otherwise have been the obvious choice. Molecular computational
  • comparison with other edges held in easily accessible memory. Once the object is identified through its edges, appropriate activation of leg muscles will enable the person to flee the scene if necessary. Edge detection can also be achieved in a semiconductor computing context, but not with a logic gate array
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Published 29 Dec 2015

Biocatalysis for the application of CO2 as a chemical feedstock

  • Apostolos Alissandratos and
  • Christopher J. Easton

Beilstein J. Org. Chem. 2015, 11, 2370–2387, doi:10.3762/bjoc.11.259

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  • enzyme reported to catalyse both formate oxidation and CO2 reduction under appropriate conditions, using substrate amounts of NAD+/NADH [119]. This enzyme was later used in the seminal work of Parkinson and Weaver [120], where electrons were supplied through a semiconductor photoelectrode using light in
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Published 01 Dec 2015

Polythiophene and oligothiophene systems modified by TTF electroactive units for organic electronics

  • Alexander L. Kanibolotsky,
  • Neil J. Findlay and
  • Peter J. Skabara

Beilstein J. Org. Chem. 2015, 11, 1749–1766, doi:10.3762/bjoc.11.191

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  • in organic field effect transistors and solar cells. Keywords: donor; oligothiophene; organic electronics; polythiophene; semiconductor; tetrathiafulvalene; Introduction Sulfur-rich π-functional systems are important building blocks in materials chemistry. Among them, tetrathiafulvalene (TTF
  • studied polythiophene materials for organic electronics are regioregular poly(3-hexylthiophene) (P3HT) [2][3] and poly(3,4-ethylenedioxythiophene) (PEDOT) [4], which is highly conductive in its doped state. P3HT has become a benchmark polymer semiconductor for both bulk hetero-junction solar cells (BHJSCs
  • from those in solution (−4.95/−3.55 eV), which suggested significant donor–acceptor interactions in the solid phase between the DPP and TTF units. OFET device fabrication employing polymer 48 exhibited p-type semiconductor behaviour, with the best performance from devices using the bottom contact top
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Published 28 Sep 2015

Preparative semiconductor photoredox catalysis: An emerging theme in organic synthesis

  • David W. Manley and
  • John C. Walton

Beilstein J. Org. Chem. 2015, 11, 1570–1582, doi:10.3762/bjoc.11.173

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  • David W. Manley John C. Walton University of St. Andrews, EaStCHEM School of Chemistry, St. Andrews, Fife, KY16 9ST, UK 10.3762/bjoc.11.173 Abstract Heterogeneous semiconductor photoredox catalysis (SCPC), particularly with TiO2, is evolving to provide radically new synthetic applications. In
  • this review we describe how photoactivated SCPCs can either (i) interact with a precursor that donates an electron to the semiconductor thus generating a radical cation; or (ii) interact with an acceptor precursor that picks up an electron with production of a radical anion. The radical cations of
  • )phthalimide was employed by the Overman group in their synthesis of (−)-aplyviolene [11]. Heterogeneous PRCs form a second class consisting of semiconductor materials. These are generally metal oxides or sulfides in the form of fine particles that consequently have the additional advantage of easily being
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Published 09 Sep 2015

Thiazole-induced rigidification in substituted dithieno-tetrathiafulvalene: the effect of planarisation on charge transport properties

  • Rupert G. D. Taylor,
  • Joseph Cameron,
  • Iain A. Wright,
  • Neil Thomson,
  • Olena Avramchenko,
  • Alexander L. Kanibolotsky,
  • Anto R. Inigo,
  • Tell Tuttle and
  • Peter J. Skabara

Beilstein J. Org. Chem. 2015, 11, 1148–1154, doi:10.3762/bjoc.11.129

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  • transistors (OFETs) Compounds 1 and 2 were used in the fabrication of bottom-gate bottom-contact OFETs to give an indication on the applicability of these small molecules to organic semiconductor devices. The use of self-assembled monolayers (SAMs) was investigated with pentafluorobenzenethiol (PFBT) and
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Published 10 Jul 2015

Impact of multivalent charge presentation on peptide–nanoparticle aggregation

  • Daniel Schöne,
  • Boris Schade,
  • Christoph Böttcher and
  • Beate Koksch

Beilstein J. Org. Chem. 2015, 11, 792–803, doi:10.3762/bjoc.11.89

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  • macrostructures. Keywords: coiled-coil peptides; α-helical fibrils; controlled aggregation; gold nanoparticles; multivalency; Introduction In the past few decades metal and semiconductor nanoparticles, including gold nanoparticles, have gained much interest due to their desirable optical, magnetic, and
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Published 15 May 2015

Synthesis of tripodal catecholates and their immobilization on zinc oxide nanoparticles

  • Franziska Klitsche,
  • Julian Ramcke,
  • Julia Migenda,
  • Andreas Hensel,
  • Tobias Vossmeyer,
  • Horst Weller,
  • Silvia Gross and
  • Wolfgang Maison

Beilstein J. Org. Chem. 2015, 11, 678–686, doi:10.3762/bjoc.11.77

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  • is a piezoelectronic semiconductor with a high exciton binding energy (60 meV) and a wide band-gap (3.37 eV) at room temperature [17][18]. ZnO is therefore employed in (bio-)sensors [19], ultraviolet (UV) light-emitting diodes [20], UV laser diodes [21] and in the field of catalysis [22][23]. ZnO
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Published 07 May 2015

Synthesis and properties of novel star-shaped oligofluorene conjugated systems with BODIPY cores

  • Clara Orofino-Pena,
  • Diego Cortizo-Lacalle,
  • Joseph Cameron,
  • Muhammad T. Sajjad,
  • Pavlos P. Manousiadis,
  • Neil J. Findlay,
  • Alexander L. Kanibolotsky,
  • Dimali Amarasinghe,
  • Peter J. Skabara,
  • Tell Tuttle,
  • Graham A. Turnbull and
  • Ifor D. W. Samuel

Beilstein J. Org. Chem. 2014, 10, 2704–2714, doi:10.3762/bjoc.10.285

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  • Strathclyde, Glasgow, G1 1XL, UK Organic Semiconductor Centre, SUPA, School of Physics & Astronomy, University of St. Andrews, St. Andrews, KY16 9SS, UK Institute of Physical-Organic Chemistry and Coal Chemistry, 83114 Donetsk, Ukraine 10.3762/bjoc.10.285 Abstract Star-shaped conjugated systems with varying
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Published 19 Nov 2014

Solution processable diketopyrrolopyrrole (DPP) cored small molecules with BODIPY end groups as novel donors for organic solar cells

  • Diego Cortizo-Lacalle,
  • Calvyn T. Howells,
  • Upendra K. Pandey,
  • Joseph Cameron,
  • Neil J. Findlay,
  • Anto Regis Inigo,
  • Tell Tuttle,
  • Peter J. Skabara and
  • Ifor D. W. Samuel

Beilstein J. Org. Chem. 2014, 10, 2683–2695, doi:10.3762/bjoc.10.283

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  • Diego Cortizo-Lacalle Calvyn T. Howells Upendra K. Pandey Joseph Cameron Neil J. Findlay Anto Regis Inigo Tell Tuttle Peter J. Skabara Ifor D. W. Samuel WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, G1 1XL, UK Organic Semiconductor Centre, SUPA, School of
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Published 18 Nov 2014

An integrated photocatalytic/enzymatic system for the reduction of CO2 to methanol in bioglycerol–water

  • Michele Aresta,
  • Angela Dibenedetto,
  • Tomasz Baran,
  • Antonella Angelini,
  • Przemysław Łabuz and
  • Wojciech Macyk

Beilstein J. Org. Chem. 2014, 10, 2556–2565, doi:10.3762/bjoc.10.267

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  • by the Kubelka–Munk function. The properties of the photocatalysts used can be summarized as follows. Cu2O is a visible-light-absorbing, red-colored, p-type semiconductor with the band gap energy equal of 2.1 eV. InVO4 is an n-type semiconductor (Ebg = 2.8 eV). TiO2 modified with the organic compound
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Published 03 Nov 2014

Influence of cyclodextrin on the UCST- and LCST-behavior of poly(2-methacrylamido-caprolactam)-co-(N,N-dimethylacrylamide)

  • Alexander Burkhart and
  • Helmut Ritter

Beilstein J. Org. Chem. 2014, 10, 1951–1958, doi:10.3762/bjoc.10.203

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  • accomplished using a TP1 turbidity photometer in a temperature range of 5 to 70 °C. During continuous stirring, the transparency of the sample was determined by a voltage-controlled semiconductor or laser and a silicon photodiode at a wavelength of 590 nm and a heating or cooling rate of 1 °C min−1. The
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Published 21 Aug 2014

Aryl substitution of pentacenes

  • Andreas R. Waterloo,
  • Anna-Chiara Sale,
  • Dan Lehnherr,
  • Frank Hampel and
  • Rik R. Tykwinski

Beilstein J. Org. Chem. 2014, 10, 1692–1705, doi:10.3762/bjoc.10.178

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  • unsymmetrical substitution on the solid-state packing of the pentacene derivatives. The obtained results add to our ability to better predict substitution patterns that might be helpful for designing new semiconductors for use in solid-state devices. Keywords: carbon-nanomaterials; organic semiconductor
  • stability, processability, and semiconductor device performance. Intermolecular π–π-interactions between chromophores can be dramatically improved upon functionalization at the 6- and 13-positions of pentacene, as demonstrated by the two-dimensional (2D) bricklayer-packing motif for TIPSPc [13][14]. A
  • number of well-designed substitution patterns for the pentacene skeleton have been realized to date [17][18][19][20][21][22][23][24][25], and pentacene derivatives that provide good semiconductor device performance often show similar 6,13-substitution patterns (Figure 1a) [12][26]. The most reactive
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Published 28 Jul 2014

Homogeneous and heterogeneous photoredox-catalyzed hydroxymethylation of ketones and keto esters: catalyst screening, chemoselectivity and dilution effects

  • Axel G. Griesbeck and
  • Melissa Reckenthäler

Beilstein J. Org. Chem. 2014, 10, 1143–1150, doi:10.3762/bjoc.10.114

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  • Axel G. Griesbeck Melissa Reckenthaler University of Cologne, Department of Chemistry, Organic Chemistry, Greinstr. 4, D-50939 Köln, Germany; Fax: +49(221)470 5057 10.3762/bjoc.10.114 Abstract The homogeneous titanium- and dye-catalyzed as well as the heterogeneous semiconductor particle
  • coupling is the dominant process for semiconductor catalysis and ketone reduction dominates the Ti(OiPr)4/methanol or isopropanol systems. Application of dilution effects on the TiO2 catalysis leads to an increase in hydroxymethylation at the expense of the pinacol coupling. Keywords: alkylation; carbonyl
  • ; photocatalysis; photoredox catalysis; redox; semiconductor; Introduction Stimulated by the principles of sustainable chemical synthesis and the progress in our understanding of catalytic and photoinduced electron-transfer processes, in recent years photoredox catalysis emerged as a new and powerful area for
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Published 19 May 2014

Organic synthesis using photoredox catalysis

  • Axel G. Griesbeck

Beilstein J. Org. Chem. 2014, 10, 1097–1098, doi:10.3762/bjoc.10.107

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  • other Ru or Ir complexes) with strong MLCT transitions, organic dyes such as xanthene, porphyrine or phthalocyanine dyes (e.g., eosin Y), and colloidal semiconductor particles (e.g., TiO2) [1][2][3][4][5][6][7][8][9]. In addition, combinations of light-absorbing materials have been studied such as dye
  • -coated semiconductor nanoparticles. On the substrate side, the focus is on redox-active donor/acceptor molecules, which range from all kind of aromatic, olefinic and carbonyl-type electron acceptor compounds to heteroatom-linked electron donors. The relevance of carbon–carbon bond formation for organic
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Published 12 May 2014

Crystal design using multipolar electrostatic interactions: A concept study for organic electronics

  • Peer Kirsch,
  • Qiong Tong and
  • Harald Untenecker

Beilstein J. Org. Chem. 2013, 9, 2367–2373, doi:10.3762/bjoc.9.272

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  • isotropic charge transport compared to the “herring bone” stacking observed for other acenes. Keywords: aromatic stacking; charge carrier transport; crystal design; electrostatic control; organic semiconductor; organo-fluorine; Introduction Within a very few years the first organic semiconductors have
  • . In contrast to Anthony’s approach of steric interference with the formation of one-dimensional stacks, our approach is based on “sculpting” the electrostatic potential surface of the semiconductor molecule in a way that cofacial stacking leads to electrostatic repulsion which can be converted into
  • electrostatically controlled crystal packing is the very poor solubility of 1. Theoretical study on electronic properties In order to explore the potential utility of 1 and its analogues as an organic semiconductor, the transfer integrals [20][21] for hole and electron transfer between the four closest pairs of
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Published 05 Nov 2013

Metal-free aerobic oxidations mediated by N-hydroxyphthalimide. A concise review

  • Lucio Melone and
  • Carlo Punta

Beilstein J. Org. Chem. 2013, 9, 1296–1310, doi:10.3762/bjoc.9.146

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  • medium-band-gap semiconductor and has proved to be an efficient photocatalyst for synthetic purposes [66][67]. It has been demonstrated that the excited state of g-C3N4, obtained by irradiation with visible light, is able to activate O2 to the corresponding superoxide radical. The latter could undergo
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Published 02 Jul 2013

Camera-enabled techniques for organic synthesis

  • Steven V. Ley,
  • Richard J. Ingham,
  • Matthew O’Brien and
  • Duncan L. Browne

Beilstein J. Org. Chem. 2013, 9, 1051–1072, doi:10.3762/bjoc.9.118

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  • later retrieval and processing. The solid-state nature of CCD (charge-coupled device) and CMOS (complementary metal–oxide–semiconductor) imaging chips means that digital cameras can be very robust, which is of significant benefit in a laboratory environment. Many devices are highly portable, being hand
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Published 31 May 2013

Influence of cyclodextrin on the solubility of a classically prepared 2-vinylcyclopropane macromonomer in aqueous solution

  • Helmut Ritter,
  • Jia Cheng and
  • Monir Tabatabai

Beilstein J. Org. Chem. 2012, 8, 1528–1535, doi:10.3762/bjoc.8.173

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  • ) instrument equipped with a He–Ne-laser and an Avalanche photodiode detector. The turbidity measurements were carried out using a power-regulated semiconductor laser (λ = 670 nm) and a silicon photodiode in a TP1 turbidity photometer from TEPPER-Analytik. Glass-transition temperatures (Tg) were measured using
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Published 13 Sep 2012

Synthesis and characterization of a novel carboxyl group containing (co)polyimide with sulfur in the polymer backbone

  • Miroslav Mrsevic,
  • David Düsselberg and
  • Claudia Staudt

Beilstein J. Org. Chem. 2012, 8, 776–786, doi:10.3762/bjoc.8.88

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  • attractive for optical lenses and optoelectronic applications, such as OLEDs (organic light-emitting diodes) or high-performance CMOS-CISs (complementary metal–oxide–semiconductor contact image sensor) [18]. Although (co)polyimides exhibit excellent properties and are numbered among the high-performance
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Published 25 May 2012
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  • range of 15 to 70 °C. During continuous stirring, the transparency of the sample was determined by a voltage controlled semiconductor laser and a silicium-photodiode at a wavelength of 500 nm and a heating or cooling rate of 1 °C·min−1. All critical temperatures were detected by determination of the
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Published 14 Feb 2011

Self-assembly and semiconductivity of an oligothiophene supergelator

  • Pampa Pratihar,
  • Suhrit Ghosh,
  • Vladimir Stepanenko,
  • Sameer Patwardhan,
  • Ferdinand C. Grozema,
  • Laurens D. A. Siebbeles and
  • Frank Würthner

Beilstein J. Org. Chem. 2010, 6, 1070–1078, doi:10.3762/bjoc.6.122

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  • studies of trialkoxybenzamide-functionalized quaterthiophene derivative T1 (Scheme 1). We also present our initial results on the morphology of blends of this electron-rich p-type semiconducting T1 with the well-known n-type semiconductor [6,6]-phenyl-C61-butyric acid methyl ester (PCBM). Results and
  • concentration of 5 x 10−5 M. Studies on blends of T1 with PCBM The fullerene derivative [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) is a well-known n-type semiconductor and its blends with various electron-donor materials have been extensively used in solar cell devices [24]. The morphology of the blend
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Published 16 Nov 2010

Redox-active tetrathiafulvalene and dithiolene compounds derived from allylic 1,4-diol rearrangement products of disubstituted 1,3-dithiole derivatives

  • Filipe Vilela,
  • Peter J. Skabara,
  • Christopher R. Mason,
  • Thomas D. J. Westgate,
  • Asun Luquin,
  • Simon J. Coles and
  • Michael B. Hursthouse

Beilstein J. Org. Chem. 2010, 6, 1002–1014, doi:10.3762/bjoc.6.113

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  • motif for materials applications. For example, benzyl and thienyl annelated TTF derivatives and analogues have been shown to perform well as semiconductor materials in organic field effect transistors (OFETs) [21][22]. This has been attributed to the enhanced π–π stacking of the extended aromatic groups
  • as precursors to highly electroactive polythiophenes [27][28]. We were interested in the self-assembly of compound 28 in the solid state to assess whether or not this material would be suitable as a semiconductor in OFETs [29]. Single crystals of compound 28 were grown from a dichloromethane/hexane
  • positions with 50% probability. The packing diagram in Figure 5 highlights the intermolecular interactions that exist in the bulk, which in turn would support semiconductor behaviour. Firstly, there are sulfur–sulfur close contacts between adjacent S7 atoms (3.2479(8) Å), and these interactions are
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Published 21 Oct 2010
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