Pure and Applied Chemistry

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• Gardarsson Haraldur, Schweizer W. Bernd, Trapp Nils, Diederich François: Structures and Properties of Molecular Torsion Balances to Decipher the Nature of Substituent Effects on the Aromatic Edge-to-Face Interaction. Chem. Eur. J. 2014, 20, 4608. <http://dx.doi.org/10.1002/chem.201304810>
• McGarry Kathryn A., Xie Wei, Sutton Christopher, Risko Chad, Wu Yanfei, Young Victor G., Brédas Jean-Luc, Frisbie C. Daniel, Douglas Christopher J.: Rubrene-Based Single-Crystal Organic Semiconductors: Synthesis, Electronic Structure, and Charge-Transport Properties. Chem. Mater. 2013, 25, 2254. <http://dx.doi.org/10.1021/cm400736s>
• Dresselhaus Thomas, Yang Jack, Kumbhar Sadhana, Waller Mark P.: Hybrid Metaheuristic Approach for Nonlocal Optimization of Molecular Systems. J. Chem. Theory Comput. 2013, 9, 2137. <http://dx.doi.org/10.1021/ct301079m>
• Raju Rajesh K., Bloom Jacob W. G., Wheeler Steven E.: Broad Transferability of Substituent Effects in π-Stacking Interactions Provides New Insights into Their Origin. J. Chem. Theory Comput. 2013, 9, 3479. <http://dx.doi.org/10.1021/ct400481r>
• Muchowska Kamila B., Adam Catherine, Mati Ioulia K., Cockroft Scott L.: Electrostatic Modulation of Aromatic Rings via Explicit Solvation of Substituents. J. Am. Chem. Soc. 2013, 135, 9976. <http://dx.doi.org/10.1021/ja402566w>
• Mati Ioulia K., Adam Catherine, Cockroft Scott L.: Seeing through solvent effects using molecular balances. Chem. Sci. 2013, 4, 3965. <http://dx.doi.org/10.1039/c3sc51764k>
• Baldridge Kim K., Cozzi Franco, Siegel Jay S.: Basicity of (2,6-Pyridino)paracyclophanes: Lone Pair-π, Cation-π, and Solvation Effects. Angew. Chem. 2012, 124, 2957. <http://dx.doi.org/10.1002/ange.201108545>
• Baldridge Kim K., Cozzi Franco, Siegel Jay S.: Basicity of (2,6-Pyridino)paracyclophanes: Lone Pair-π, Cation-π, and Solvation Effects. Angew. Chem. Int. Ed. 2012, 51, 2903. <http://dx.doi.org/10.1002/anie.201108545>
• Xia Jian Long, Liu Sheng Hua, Cozzi Franco, Mancinelli Michele, Mazzanti Andrea: An Experimental Study on the Effect of Substituents on Aromatic-Aromatic Interactions in Dithia[3,3]-metaparacyclophanes. Chemistry A European Journal 2012, 18, 3611. <http://dx.doi.org/10.1002/chem.201103639>
• Lima Carlos F. R. A. C., Rocha Marisa A. A., Gomes Lígia R., Low John N., Silva Artur M. S., Santos Luís M. N. B. F.: Experimental Support for the Role of Dispersion Forces in Aromatic Interactions. Chem. Eur. J. 2012, 18, 8934. <http://dx.doi.org/10.1002/chem.201201056>
• Snyder Seth E., Huang Bin-Syuan, Chu Yu W., Lin Huei-Shian, Carey James R.: The Effects of Substituents on the Geometry of π-π Interactions. Chem. Eur. J. 2012, 18, 12663. <http://dx.doi.org/10.1002/chem.201202253>
• Lima Carlos F. R. A. C., Gomes Lígia R., Low John N., Silva Artur M. S., Santos Luís M. N. B. F.: Elucidating the Role of Aromatic Interactions in Rotational Barriers Involving Aromatic Systems. J. Org. Chem. 2012, 77, 10422. <http://dx.doi.org/10.1021/jo301629y>
• Lima Carlos F. R. A. C., Rocha Marisa A. A., Schröder Bernd, Gomes Lígia R., Low John N., Santos Luís M. N. B. F.: Phenylnaphthalenes: Sublimation Equilibrium, Conjugation, and Aromatic Interactions. Chem B 2012, 116, 3557. <http://dx.doi.org/10.1021/jp2111378>
• Moorthy Jarugu Narasimha, Mandal Susovan, Parida Keshaba Nanda: Through-Space Control of the Persistence of Photogenerated o-Quinonoid Intermediates in Naphthalenes Containing Cofacially Oriented Chromenes and Arenes^‡. Z Org Lett 2012, 14, 2438. <http://dx.doi.org/10.1021/ol300449p>
• Raju Rajesh K., Bloom Jacob W. G., An Yi, Wheeler Steven E.: Substituent Effects on Non-Covalent Interactions with Aromatic Rings: Insights from Computational Chemistry. chem phys chem 2011, 12, 3116. <http://dx.doi.org/10.1002/cphc.201100542>
• Lambert Stephanie G., Asenstorfer Robert E., Williamson Natalie M., Iland Patrick G., Jones Graham P.: Copigmentation between malvidin-3-glucoside and some wine constituents and its importance to colour expression in red wine. Food Chem 2011, 125, 106. <http://dx.doi.org/10.1016/j.foodchem.2010.08.045>
• Li Gao-Qiang, Yamamoto Yasunori, Miyaura Norio: Double-coupling of dibromo arenes with aryltriolborates for synthesis of diaryl-substituted planar frameworks. Tetrahed 2011, 67, 6804. <http://dx.doi.org/10.1016/j.tet.2011.06.083>
• Wheeler Steven E.: Local Nature of Substituent Effects in Stacking Interactions. J Am Chem Soc 2011, 133, 10262. <http://dx.doi.org/10.1021/ja202932e>
• Ghosn Marwan W., Wolf Christian: Synthesis, Conformational Stability, and Asymmetric Transformation of Atropisomeric 1,8-Bisphenolnaphthalenes. J Org Chem 2011, 76, 3888. <http://dx.doi.org/10.1021/jo200309g>
• Avasthi Kamlakar, Ansari Amantullah, Kant Ruchir, Maulik Prakas R., Ravikumar Krishnan, Chattopadhyay Partha, Adhikary Nirmal D.: An alternative to ‘propylene/Leonard linker’ for studying arene interactions in flexible pyrazolo[3,4-d]pyrimidine core based models both at molecular and supramolecular levels. CrystEngCommun 2011, 13, 2039. <http://dx.doi.org/10.1039/c0ce00336k>
• Josa Daniela, Otero Jesús Rodríguez, Cabaleiro Lago Enrique M.: A DFT study of substituent effects in corannulene dimers. PCCP 2011, 13, 21139. <http://dx.doi.org/10.1039/c1cp23021b>
• Benaglia Maurizio, Cozzi Franco, Mancinelli Michele, Mazzanti Andrea: The Intramolecular Interaction of Thiophene and Furan with Aromatic and Fluoroaromatic Systems in Some [3.3]Meta(heterocyclo)paracyclophanes: A Combined Computational and NMR Spectroscopic Study. Chem Eur J 2010, 16, 7456. <http://dx.doi.org/10.1002/chem.201000783>
• Wheeler Steven E., McNeil Anne J., Müller Peter, Swager Timothy M., Houk K. N.: Probing Substituent Effects in Aryl−Aryl Interactions Using Stereoselective Diels−Alder Cycloadditions. J Am Chem Soc 2010, 132, 3304. <http://dx.doi.org/10.1021/ja903653j>
• Mati Ioulia K., Cockroft Scott L.: Molecular balances for quantifying non-covalent interactions. Chem Soc Rev 2010, 39, 4195. <http://dx.doi.org/10.1039/b822665m>
• Karim Arif R., Linden Anthony, Baldridge Kim K., Siegel Jay S.: Symmetry and polar-π effects on the dynamics of enshrouded aryl-alkyne molecular rotors. Chem Sci 2010, 1, 102. <http://dx.doi.org/10.1039/c0sc00117a>
• Baker Matthew B., Yuan Ling, Marth Christopher J., Li Yan, Castellano Ronald K.: Rapid access to C ₃- and C _s-symmetric AAT organogelators via ring opening of a common benzotrifuranone precursor. Supramol Chem 2010, 22, 789. <http://dx.doi.org/10.1080/10610278.2010.500733>
• Yoon Il, Benítez Diego, Zhao Yan-Li, Miljanić Ognjen Š., Kim Soo-Young, Tkatchouk Ekaterina, Leung Ken C.-F., Khan Saeed I., Goddard William A., Stoddart J. Fraser: Functionally Rigid and Degenerate Molecular Shuttles. Chem Eur J 2009, 15, 1115. <http://dx.doi.org/10.1002/chem.200802096>
• Annunziata Rita, Benaglia Maurizio, Cozzi Franco, Mazzanti Andrea: The Intramolecular Edge-to-Face Interactions of an Aryl CH Bond and of a Pyridine Nitrogen Lone-Pair with Aromatic and Fluoroaromatic Systems in Some [3,3]Metaparacyclophanes: A Combined Computational and NMR Study. Chem Eur J 2009, 15, 4373. <http://dx.doi.org/10.1002/chem.200802490>
• Roussel Christian, Kaid-Slimane Radia, Andreoli Federico, Renaudin Mailis, Vanthuyne Nicolas: Synthesis, chiral separation, and absolute configuration of bis-(N-aryl) atropisomeric triads: 1,2-Bis-[4-methyl-2-(thi)oxo-2,3-dihydrothiazol-3-yl]-benzene. Chirality 2009, 21, 160. <http://dx.doi.org/10.1002/chir.20599>
• Shimazaki Yuichi, Yajima Tatsuo, Takani Masako, Yamauchi Osamu: Metal complexes involving indole rings: Structures and effects of metal–indole interactions. Coord Chem Rev - 2009, 253, 479. <http://dx.doi.org/10.1016/j.ccr.2008.04.012>
• Hammud Hassan H., Holman K. Travis, Masoud Mamdouh S., El-Faham Ayman, Beidas Hanan: 1-Hydroxybenzotriazole (HOBt) acidity, formation constant with different metals and thermodynamic parameters: Synthesis and characterization of some HOBt metal complexes – Crystal structures of two polymers: [Cu2(H2O)5(OBt)2(μ-OBt)2]·2H2O·EtOH (1A) and [Cu(μ-OBt)(HOBt)(OBt)(EtOH)] (1B). Inorg Chim Ada 2009, 362, 3526. <http://dx.doi.org/10.1016/j.ica.2009.03.046>
• Shu Lijin, Müri Marcel, Krupke Ralph, Mayor Marcel: Shape-persistent macrocycles comprising perfluorinated benzene subunits: synthesis, aggregation behaviour and unexpected μ-rod formation. Org Biomol Chem 2009, 7, 1081. <http://dx.doi.org/10.1039/b817274a>
• Shimazaki Yuichi, Takani Masako, Yamauchi Osamu: Metal complexes of amino acids and amino acid side chain groups. Structures and properties. Dalton Trans 2009, 7854. <http://dx.doi.org/10.1039/b905871k>
• Dell'Anna Gian Maria, Annunziata Rita, Benaglia Maurizio, Celentano Giuseppe, Cozzi Franco, Francesconi Oscar, Roelens Stefano: Aromatic tripodal receptors for (C60-Ih)[5,6]fullerene. Org Biomol Chem 2009, 7, 3871. <http://dx.doi.org/10.1039/b910921h>
• Duttwyler Simon, Do Quyen-Quyen, Linden Anthony, Baldridge Kim K., Siegel Jay S.: Synthesis of 2,6-Diarylphenyldimethylsilyl Cations: Polar-π Distribution of Cation Character. Angew Chem 2008, 120, 1743. <http://dx.doi.org/10.1002/ange.200705291>
• Duttwyler Simon, Do Quyen-Quyen, Linden Anthony, Baldridge Kim K., Siegel Jay S.: Synthesis of 2,6-Diarylphenyldimethylsilyl Cations: Polar-π Distribution of Cation Character. Angew Chem Int Ed 2008, 47, 1719. <http://dx.doi.org/10.1002/anie.200705291>
• Zahn Alain, Leumann Christian J.: Recognition Properties of Donor- and Acceptor-Modified Biphenyl-DNA. Chem Eur J 2008, 14, 1087. <http://dx.doi.org/10.1002/chem.200701345>
• Tewari Ashish Kumar, Dubey Rashmi: Emerging trends in molecular recognition: Utility of weak aromatic interactions. biorg med chem 2008, 16, 126. <http://dx.doi.org/10.1016/j.bmc.2007.09.023>
• Sonoda Motohiro, Yamaguchi Yui, Tahara Kazukuni, Hirose Keiji, Tobe Yoshito: Solvophobically driven self-association of a butadiyne-bridged pyridine macrocycle. Tetrahedron 2008, 64, 11490. <http://dx.doi.org/10.1016/j.tet.2008.08.058>
• Arnstein Stephen A., Sherrill C. David: Substituent effects in parallel-displaced π–π interactions. Phys Chem Chem Phys 2008, 10, 2646. <http://dx.doi.org/10.1039/b718742d>
• Cozzi Franco, Annunziata Rita, Benaglia Maurizio, Baldridge Kim K., Aguirre Gerardo, Estrada Jesús, Sritana-Anant Yongsak, Siegel Jay S.: Through-space interactions between parallel-offset arenes at the van der Waals distance: 1,8-diarylbiphenylene syntheses, structure and QM computations. Phys Chem Chem Phys 2008, 10, 2686. <http://dx.doi.org/10.1039/b800031j>
• Yoon Il, Miljanić Ognjen Š., Benítez Diego, Khan Saeed I., Stoddart J. Fraser: An interdigitated functionally rigid [2]rotaxane. Chem Commun 2008, 4561. <http://dx.doi.org/10.1039/b808005d>
• Suzuki Takanori, Tanaka Shoko, Kawai Hidetoshi, Fujiwara Kenshu: Multi-input–Multi-output Molecular Response System Based on Dynamic Redox Behavior of Hexaphenylethane-type Electron Donors with the Tetrahydrophenanthrazepine Skeleton: Strong Chiroptical Signals through the Transmission of Point Chirality to Helicity. Chem Asian J 2007, 2, 171. <http://dx.doi.org/10.1002/asia.200600299>
• Zaworotko Michael J., Hammud Hassan H., Kravtsov Victor Ch.: The co-crystal of iron(II) complex hydrate with hydroxybenzoic acid: [Fe(Phen)3]Cl(p-hydroxybenzoate).2(p-hydroxybenzoic acid).7H2O. J Chem Crystallogr 2007, 37, 219. <http://dx.doi.org/10.1007/s10870-006-9174-5>
• Mooibroek Tiddo J., Gamez Patrick: The s-triazine ring, a remarkable unit to generate supramolecular interactions. Inorg Chim Ada 2007, 360, 381. <http://dx.doi.org/10.1016/j.ica.2006.07.061>
• Lavecchia Antonio, Cosconati Sandro, Novellino Ettore, Calleri Enrica, Temporini Caterina, Massolini Gabriella, Carbonara Giuseppe, Fracchiolla Giuseppe, Loiodice Fulvio: Exploring the molecular basis of the enantioselective binding of penicillin G acylase towards a series of 2-aryloxyalkanoic acids: A docking and molecular dynamics study. Mol Graph Model 2007, 25, 773. <http://dx.doi.org/10.1016/j.jmgm.2006.07.001>
• Yajima Tatsuo, Takamido Reiko, Shimazaki Yuichi, Odani Akira, Nakabayashi Yasuo, Yamauchi Osamu: ??? Stacking assisted binding of aromatic amino acids by copper(ii)?aromatic diimine complexes. Effects of ring substituents on ternary complex stability. Dalton Trans 2007, 299. <http://dx.doi.org/10.1039/b612394e>
• Cockroft Scott L., Perkins Julie, Zonta Cristiano, Adams Harry, Spey Sharon E., Low Caroline M. R., Vinter Jeremy G., Lawson Kevin R., Urch Christopher J., Hunter Christopher A.: Substituent effects on aromatic stacking interactions. Org Biomol Chem 2007, 5, 1062. <http://dx.doi.org/10.1039/b617576g>
• Kang Seogshin, Aprahamian Ivan, Stoddart J. Fraser: Pirouetting in chiral [2]catenanes. Isr J Chem 2007, 47, 253. <http://dx.doi.org/10.1560/IJC.47.2.253>
• Massolini Gabriella, Fracchiolla Giuseppe, Calleri Enrica, Carbonara Giuseppe, Temporini Caterina, Lavecchia Antonio, Cosconati Sandro, Novellino Ettore, Loiodice Fulvio: Elucidation of the enantioselective recognition mechanism of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxy-2-arylacetic acids. Chirality 2006, 18, 633. <http://dx.doi.org/10.1002/chir.20300>
• Balaban Teodor Silviu, Eichhöfer Andreas, Krische Michael J., Lehn Jean-Marie: Hierarchic Supramolecular Interactions within Assemblies in Solution and in the Crystal of 2,3,6,7-Tetrasubstituted 5,5′-(Anthracene-9,10-diyl)bis[pyrimidin-2-amines]. HCA 2006, 89, 333. <http://dx.doi.org/10.1002/hlca.200690037>
• Caira Mino R., Jacobs Ayesha, Nassimbeni Luigi R., Toda Fumio: Complexation with diol host compounds. Part 36: inclusion compounds of 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol with benzene, toluene and mesitylene. J Chem Crystallogr 2006, 36, 435. <http://dx.doi.org/10.1007/s10870-005-9042-8>
• Zahn Alain, Brotschi Christine, Leumann Christian J.: Pentafluorophenyl-Phenyl Interactions in Biphenyl-DNA. Chem Eur J 2005, 11, 2125. <http://dx.doi.org/10.1002/chem.200401128>
• Mashraqui Sabir H., Sangvikar Yogesh, Ashraf Mohamed, Kumar Sukeerthi, Dâub Elise Trân Huu: Dipyridyl/pyridinium thieno[2,3-b]thiophenes as new atropisomeric systems. Synthesis, conformational analysis and energy minimization. Tetrahedron 2005, 61, 3507. <http://dx.doi.org/10.1016/j.tet.2005.01.123>
• Liu Jin, Wendt Natalie L., Boarman Kelly J.: Trifluoromethyl Groups in Crystal Design of 1,4-Diphenyl-1,3-butadienes for Topochemical [2 + 2] Photodimerization. Org Lett 2005, 7, 1007. <http://dx.doi.org/10.1021/ol0475111>
• Kabbani Ahmad T., Zaworotko Michael J., Abourahma Heba, Walsh Rosa D. Baily, Hammud Hassan H.: Supramolecular structure of tetrakis-μ-(4-chloro-3-nitrobenzoato)-bis(methanol)dicopper(II). J Chem Crystallogr 2004, 34, 749. <http://dx.doi.org/10.1007/s10870-004-7650-3>
• Busch Alexandrine, Gautheron Chapoulaud Valérie, Audoux Jérôme, Plé Nelly, Turck Alain: Synthesis of 4,5-diarylquinazolines: a system with cofacial aromatic rings. Diazines. Part 39. Tetrahedron 2004, 60, 5373. <http://dx.doi.org/10.1016/j.tet.2004.04.065>
• Kawai Hidetoshi, Nagasu Takayuki, Takeda Takashi, Fujiwara Kenshu, Tsuji Takashi, Ohkita Masakazu, Nishida Jun-ichi, Suzuki Takanori: peri-Interaction between diarylmethyl and diarylmethylium units in 1,8-disubstituted naphthalenes: preference of localized structure for the C–H bridged carbocation. Tetrahetron Lett 2004, 45, 4553. <http://dx.doi.org/10.1016/j.tetlet.2004.04.002>
• Vignon Scott A., Wong Jason, Tseng Hsian-Rong, Stoddart J. Fraser: Helical Chirality in Donor-Acceptor Catenanes^†. Org Lett 2004, 6, 1095. <http://dx.doi.org/10.1021/ol0364881>
• Manojkumar T. K., Choi H. S., Hong B. H., Tarakeshwar P., Kim K. S.: p-benzoquinone-benzene clusters as potential nanomechanical devices: A theoretical study. J Chem Phys 2004, 121, 841. <http://dx.doi.org/10.1063/1.1760745>
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• Suzuki Takanori, Nagasu Takayuki, Kawai Hidetoshi, Fujiwara Kenshu, Tsuji Takashi: Formation of keto-carbeniums from 1,2,2-triarylacenaphthen-1-ols by breaking a long CC bond: unusual alcohol protonolysis accompanied by formal hydride abstraction. Tetrahetron Lett 2003, 44, 6095. <http://dx.doi.org/10.1016/S0040-4039(03)01459-X>
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• In Yasuko, Kishima Shouitirou, Minoura Katsuhiko, Nose Takeru, Shimohigashi Yasuyuki, Ishida Toshimasa: Aggregation Feature of Fluorine-Substituted Benzene Rings and Intermolecular C–H···F Interaction: Crystal Structure Analyses of Mono- and Trifluoro-L-phenylalanines. Chem Pharm Bull 2003, 51, 1258. <http://dx.doi.org/10.1248/cpb.51.1258>
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