Pure and Applied Chemistry

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• Bunz Uwe H. F., Menning Sebastian, Martín Nazario: para-Verknüpfte Cyclophenylene und halbkugelförmige Polyarene: Bausteine für einwandige Kohlenstoffnanoröhren?. Angew. Chem. 2012, 124, 7202. <http://dx.doi.org/10.1002/ange.201201494>
• Bunz Uwe H. F., Menning Sebastian, Martín Nazario: para-Connected Cyclophenylenes and Hemispherical Polyarenes: Building Blocks for Single-Walled Carbon Nanotubes?. Angew. Chem. Int. Ed. 2012, 51, 7094. <http://dx.doi.org/10.1002/anie.201201494>
• Kupka Teobald, Chełmecka Elżbieta, Pasterny Karol, Stachów Michał, Stobiński Leszek: DFT calculations of structures, 13C NMR chemical shifts, and Raman RBM mode of simple models of small-diameter zigzag (4,0) carboxylated single-walled carbon nanotubes : Structures, 13C NMR chemical shifts, and Raman RBM mode. Magnet Reson Chem 2012, 50, 142. <http://dx.doi.org/10.1002/mrc.2874>
• Kupka Teobald, Stach��w Micha��, Che��mecka El��bieta, Pasterny Karol, Stobi��ski Leszek: DFT calculations of structures, 13C NMR chemical shifts and Raman RBM mode of simple models of ultra small diameter (4,0) zigzag hydroxylated single wall carbon nanotubes. Synthetic Metals 2012, 162, 573. <http://dx.doi.org/10.1016/j.synthmet.2012.02.002>
• Cheng Hanchao, Yang Dingqiao: Iridium-Catalyzed Asymmetric Ring-Opening of Oxabenzonorbornadienes with Phenols. J. Org. Chem. 2012, 77, 9756. <http://dx.doi.org/10.1021/jo3018507>
• Mercuri Francesco, Baldoni Matteo, Sgamellotti Antonio: Towards nano-organic chemistry: perspectives for a bottom-up approach to the synthesis of low-dimensional carbon nanostructures. Nanoscale 2012, 4, 369. <http://dx.doi.org/10.1039/c1nr11112d>
• Kupka Teobald, Stachów Michał, Nieradka Marzena, Stobiński Leszek: DFT calculation of structures and NMR chemical shifts of simple models of small diameter zigzag single wall carbon nanotubes (SWCNTs). Magn Reson Chem 2011, n/a. <http://dx.doi.org/10.1002/mrc.2777>
• Pavlov Mikhail, Ermilov Alexander: The electronic terms of the finite-length nanotubes, generated by edge states: A CASSCF study. Int J Quantum Chem 2011, 111, 2592. <http://dx.doi.org/10.1002/qua.22650>
• Omachi Haruka, Matsuura Sanae, Segawa Yasutomo, Itami Kenichiro: A Modular and Size-Selective Synthesis of [n]Cycloparaphenylenes: A Step toward the Selective Synthesis of [n,n] Single-Walled Carbon Nanotubes. angew chemie 2010, 122, 10400. <http://dx.doi.org/10.1002/ange.201005734>
• Omachi Haruka, Matsuura Sanae, Segawa Yasutomo, Itami Kenichiro: A Modular and Size-Selective Synthesis of [n]Cycloparaphenylenes: A Step toward the Selective Synthesis of [n,n] Single-Walled Carbon Nanotubes. Angew Chem Int Ed 2010, 49, 10202. <http://dx.doi.org/10.1002/anie.201005734>
• GIRRESER U., GIUFFRIDA D., KOHNKE F. H., MATHIAS J. P., PHILP D., STODDART J. F.: ChemInform Abstract: The Structure-Directed Synthesis of Cyclacene and Polyacene Derivatives. ChemInform 2010, 24, no. <http://dx.doi.org/10.1002/chin.199315324>
• Jasti Ramesh, Bertozzi Carolyn R.: Progress and challenges for the bottom-up synthesis of carbon nanotubes with discrete chirality. chem phys letts 2010, 494, 1. <http://dx.doi.org/10.1016/j.cplett.2010.04.067>
• Eisenberg David, Shenhar Roy, Rabinovitz Mordecai: Synthetic approaches to aromatic belts: building up strain in macrocyclic polyarenes. Chem Soc Rev 2010, 39, 2879. <http://dx.doi.org/10.1039/b904087k>
• Merner Bradley L., Dawe Louise N., Bodwell Graham J.: 1,1,8,8-Tetramethyl[8](2,11)teropyrenophane: Half of an Aromatic Belt and a Segment of an (8,8) Single-Walled Carbon Nanotube. Angew Chem 2009, 121, 5595. <http://dx.doi.org/10.1002/ange.200806363>
• Merner Bradley L., Dawe Louise N., Bodwell Graham J.: 1,1,8,8-Tetramethyl[8](2,11)teropyrenophane: Half of an Aromatic Belt and a Segment of an (8,8) Single-Walled Carbon Nanotube. Angew Chem Int Ed 2009, 48, 5487. <http://dx.doi.org/10.1002/anie.200806363>
• Nishiuchi Tomohiko, Kuwatani Yoshiyuki, Nishinaga Tohru, Iyoda Masahiko: Dynamic Molecular Tweezers Composed of Dibenzocyclooctatetraene Units: Synthesis, Properties, and Thermochromism in Host-Guest Complexes. Chem Eur J 2009, 15, 6838. <http://dx.doi.org/10.1002/chem.200900623>
• Howell Jennifer, Goddard John D., Tam William: A relative approach for determining ring strain energies of heterobicyclic alkenes. Tetrahedron 2009, 65, 4562. <http://dx.doi.org/10.1016/j.tet.2009.03.090>
• Johnson Carey J., Zoellner Robert W., Wu Junyong, Yan Hua, Cao Weiliang, Tantirungrotechai Yuthana, Roddecha Supacharee, Punyain Kraiwan, Toochinda Pisanu: The smallest borazine-fused cyclacenes: Novel N���H conformations in cyclo-BN-anthracene and cyclo-BN-tetracene from Hartree-Fock and density functional calculations. Journal of Molecular Structure: THEOCHEM 2009, 893, 9. <http://dx.doi.org/10.1016/j.theochem.2008.09.012>
• Balashov A. M., Ermilov A. Yu., Scherbinin A. V.: Lithium mobility in complexes Li[C_n]₁ (n = 5−21): PES analysis in different stationary points. Int J Quantum Chem 2008, 108, 2693. <http://dx.doi.org/10.1002/qua.21730>
• Stoddart J. Fraser, Colquhoun Howard M.: Big and little Meccano. Tetrahedron 2008, 64, 8231. <http://dx.doi.org/10.1016/j.tet.2008.06.035>
• Matsuo Yutaka: Creation of Cyclic π-Electron-Conjugated Systems through the Functionalization of Fullerenes and Synthesis of Their Multinuclear Metal Complexes. Bull Chem Soc Jpn 2008, 81, 320. <http://dx.doi.org/10.1246/bcsj.81.320>
• Stuparu Mihaiela, Lentz Dieter, Rüegger Heinz, Schlüter A. Dieter: Exploring the Chemistry of a Double-Stranded Cycle with the Carbon Skeleton of the Belt Region of the C84 Fullerene. Eur J Org Chem 2007, 2007, 88. <http://dx.doi.org/10.1002/ejoc.200600698>
• Sony Priya, Shukla Alok: Large-scale correlated calculations of linear optical absorption and low-lying excited states of polyacenes: Pariser-Parr-Pople Hamiltonian. Phys Rev B 2007, 75, 155208. <http://dx.doi.org/10.1103/PhysRevB.75.155208>
• Knežević Andrea, Maksić Zvonimir B.: The absolute proton affinity and the second order hyperpolarizability of some catacondensed linear polyacenes and pericondensed zethrenes. New J Chem 2006, 30, 215. <http://dx.doi.org/10.1039/b514624k>
• Eckert-Maksić Mirjana, Margetić Davor, Kirin Srećko, Milić Dalibor, Matković-Čalogović Dubravka: High-Pressure Assisted Synthesis of Fused Norbornenes Containing Two7-Metallonorbornene Units. Eur J Org Chem 2005, 2005, 4612. <http://dx.doi.org/10.1002/ejoc.200500377>
• Matsumoto Kiyoshi, Hamana Hiroshi, Iida Hirokazu: Compendium of Cycloaddition Reactions under High Pressure. HCA 2005, 88, 2033. <http://dx.doi.org/10.1002/hlca.200590156>
• Schleyer Paul von Ragué, Manoharan Mariappan, Jiao Haijun, Stahl Frank: The Acenes:  Is There a Relationship between Aromatic Stabilization and Reactivity?. Org Lett 2001, 3, 3643. <http://dx.doi.org/10.1021/ol016553b>
• Mayer Axel, Meier Herbert: 1,4-Epoxyarenes for the Generation of Molecular Ribbons. J Prakt Chem 1997, 339, 679. <http://dx.doi.org/10.1002/prac.199733901124>
• Oliver Kappe C., Shaun Murphree S., Padwa Albert: Synthetic applications of furan Diels-Alder chemistry. Tetrahedron 1997, 53, 14179. <http://dx.doi.org/10.1016/S0040-4020(97)00747-3>
• Cory Robert M., McPhail Cameron L., Dikmans Antonius J., Vittal Jagadese J.: Macrocyclic cyclophane belts via double Diels-Alder cycloadditions: Macroannulation of bisdienes by bisdienophiles. Synthesis of a key precursor to an [8]cyclacene. Tetrahetron Lett 1996, 37, 1983. <http://dx.doi.org/10.1016/0040-4039(96)00263-8>
• Gutman Ivan, Biedermann P. Ulrich, Ivanov-Petrović Vesna, Agranat Israel: Cyclic Conjugation Effects in Cyclacenes. Polycyclic Arom Comp 1996, 8, 189. <http://dx.doi.org/10.1080/10406639608048345>
• Cory Robert M., McPhail Cameron L., Dikmans Antonius J.: Linearly fused ribbons of carbocyclic six-membered rings via Diels-Alder cycloadditions 1. Model studies and key intermediates. Tetrahetron Lett 1993, 34, 7533. <http://dx.doi.org/10.1016/S0040-4039(00)60392-1>
• Ashton Peter R., Brown George R., Smith Diane R., Stoddart J.Fraser, Williams David J.: Stereoselectivity in the synthesis of polyacene derivatives by repetitive Diels-Alder reactions. Tetrahetron Lett 1993, 34, 8337. <http://dx.doi.org/10.1016/S0040-4039(00)61425-9>