Pure and Applied Chemistry

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• Liang Wenrui, Zhao Zhi, Zhang Yang, Wang Qiusheng, Zhao Xin, Ouyang Jie: Highly selective detection of glutathione using a NIP/Cu2+ complex fluorescent probe. J of Lumin 2012, 132, 1160. <http://dx.doi.org/10.1016/j.jlumin.2011.12.029>
• Knoll Wolfgang, Kaneno Daisuke, Bobek Michael M., Brecker Lothar, Rosenberg Murray G., Tomoda Shuji, Brinker Udo H.: Intra- and Intermolecular Reaction Selectivities of γ-Substituted Adamantanylidenes. J Org Chern 2012, 77, 1340. <http://dx.doi.org/10.1021/jo202132c>
• Coskun Ali, Banaszak Michal, Astumian R. Dean, Stoddart J. Fraser, Grzybowski Bartosz A.: Great expectations: can artificial molecular machines deliver on their promise?. Chemical Society Review 2012, 41, 19. <http://dx.doi.org/10.1039/c1cs15262a>
• Zimmer Lucie E., Sparr Christof, Gilmour Ryan: Konformative Fluoreffekte in der Organokatalyse: eine neuartige Strategie zum molekularen Design. angew chemie 2011, 123, 12062. <http://dx.doi.org/10.1002/ange.201102027>
• Mayr Herbert, Breugst Martin, Ofial Armin R.: Farewell to the HSAB Treatment of Ambident Reactivity. Angewandte Chemie-Int Ed 2011, 50, 6470. <http://dx.doi.org/10.1002/anie.201007100>
• Zimmer Lucie E., Sparr Christof, Gilmour Ryan: Fluorine Conformational Effects in Organocatalysis: An Emerging Strategy for Molecular Design. Angew Chem Int E 2011, 50, 11860. <http://dx.doi.org/10.1002/anie.201102027>
• Wathen Brent, Pratt Derek A., Jia Zongchao: Hyperconjugation Contributes to the Bimodal Distribution of Glycine Conformations Observed in Protein Three-Dimensional Structures. Chem Eur J of Chem Bio 2011, 12, 1674. <http://dx.doi.org/10.1002/cbic.201100156>
• Laurence Christian, Graton Jérôme, Berthelot Michel, El Ghomari Mohamed J.: The Diiodine Basicity Scale: Toward a General Halogen-Bond Basicity Scale. Chemistry A European Journal 2011, 17, 10431. <http://dx.doi.org/10.1002/chem.201101071>
• Schoenebeck Franziska, Anstaett Philipp: Reductive Elimination of ArCF3 from Bidentate PdII Complexes: A Computational Study. Chemistry A European Journal 2011, 17, 12340. <http://dx.doi.org/10.1002/chem.201101373>
• Rashid Zahid, van Lenthe Joop H.: Generation of Kekulé valence structures and the corresponding valence bond wave function. J Comput Chem 2011, 32, 696. <http://dx.doi.org/10.1002/jcc.21655>
• Li Zhaohui, Hong Hanlie, Liao Libing, Ackley Caren J., Schulz Laura A., MacDonald Roberta A., Mihelich Amanda L., Emard Shannon M.: A mechanistic study of ciprofloxacin removal by kaolinite. Colloids Surface B 2011, 88, 339. <http://dx.doi.org/10.1016/j.colsurfb.2011.07.011>
• Mala’bi Tahani, Pogodin Sergey, Agranat Israel: Kinetic control wins out over thermodynamic control in Friedel–Crafts acyl rearrangements. Tetrahetron Lett 2011, 52, 1854. <http://dx.doi.org/10.1016/j.tetlet.2011.02.026>
• Hallett Jason P., Welton Tom: Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2. Chem Rev 2011, 111, 3508. <http://dx.doi.org/10.1021/cr1003248>
• Laurence Christian, Graton Jérôme, Gal Jean-François: An Overview of Lewis Basicity and Affinity Scales. J Chem Ed 2011, 88, 1651. <http://dx.doi.org/10.1021/ed200057b>
• Smith Amos B., Risatti Christina A., Atasoylu Onur, Bennett Clay S., Liu Junke, Cheng Hongsheng, TenDyke Karen, Xu Qunli: Design, Synthesis, and Biological Evaluation of Diminutive Forms of (+)-Spongistatin 1: Lessons Learned. J Am Chcm Soc 2011, 110812093240056. <http://dx.doi.org/10.1021/ja2046167>
• Maccarrone Giuseppe, Di Bella Santo, Oliveri Ivan Pietro: A Lewis Basicity Scale in Dichloromethane for Amines and Common Nonprotogenic Solvents Using a Zinc(II) Schiff-Base Complex as Reference Lewis Acid. J Org Chern 2011, 76, 8879. <http://dx.doi.org/10.1021/jo2016218>
• Klein Regina, Zech Oliver, Maurer Eva, Kellermeier Matthias, Kunz Werner: Oligoether Carboxylates: Task-Specific Room-Temperature Ionic Liquids. Chem B 2011, 115, 8961. <http://dx.doi.org/10.1021/jp200624g>
• Smith Ashlyn P., McKercher Adrienne E., Mawhinney Robert C.: Inductive Effect: A Quantum Theory of Atoms in Molecules Perspective. J Phys Chem A 2011, 115, 12544. <http://dx.doi.org/10.1021/jp202757p>
• Melko Joshua J., Werner Ute, Mitrić Roland, Bonačić-Koutecký Vlasta, Castleman A. W.: Electronic Structure Similarities in Pb_xSb_y^– and Sn_xBi_y^– Clusters. J Phys Chem A 2011, 110826122320036. <http://dx.doi.org/10.1021/jp207474h>
• Ferguson Andrew J., Kopidakis Nikos, Shaheen Sean E., Rumbles Garry: Dark Carriers, Trapping, and Activation Control of Carrier Recombination in Neat P3HT and P3HT:PCBM Blends. J Phys Chem C 2011, 111102094541002. <http://dx.doi.org/10.1021/jp208014v>
• Schreiner P. R., Reisenauer H. P., Ley D., Gerbig D., Wu C.-H., Allen W. D.: Methylhydroxycarbene: Tunneling Control of a Chemical Reaction. Sci 2011, 332, 1300. <http://dx.doi.org/10.1126/science.1203761>
• Li Feng, Jennings James Robert, Mathews Nripan, Wang Qing: Evolution of Charge Collection ∕ Separation Efficiencies in Dye-Sensitized Solar Cells Upon Aging: A Case Study. Electrochemical Society 2011, 158, B1158. <http://dx.doi.org/10.1149/1.3610366>
• Braslavsky Silvia E., Braun André M., Cassano Alberto E., Emeline Alexei V., Litter Marta I., Palmisano Leonardo, Parmon Valentin N., Serpone Nick: Glossary of terms used in photocatalysis and radiation catalysis (IUPAC Recommendations 2011). Pure and App Chemis 2011, 1. <http://dx.doi.org/10.1351/PAC-REC-09-09-36>
• Kemnitz Carl R., Mackey Joel L., Loewen Mark J., Hargrove Julie L., Lewis Joshua L., Hawkins Whitney E., Nielsen Adam F.: Origin of Stability in Branched Alkanes. Chem Eur J 2010, 16, 6942. <http://dx.doi.org/10.1002/chem.200902550>
• Guerrero Andrés, Herrero Rebeca, Quintanilla  Esther, Dávalos Juan Z., Abboud José-Luis M., Coto Pedro B., Lenoir Dieter: Single-Electron Self-Exchange between Cage Hydrocarbons and Their Radical Cations in the Gas Phase. Chem Eur J of Chem Phys 2010, 11, 713. <http://dx.doi.org/10.1002/cphc.200900824>
• Bougherara Habiba, Klika Václav, Maršík František, Mařík Ivo A., Yahia L'Hocine: New predictive model for monitoring bone remodeling. J Biomed Mater Res 2010, 95a, 9. <http://dx.doi.org/10.1002/jbm.a.32679>
• Reichardt Christian: Lösungsmittelpolarität-Was ist das?. Nachr Chem Tech Lab 2010, 45, 759. <http://dx.doi.org/10.1002/nadc.19970450710>
• Couzijn Erik P. A., Slootweg J. Chris, Ehlers Andreas W., Lammertsma Koop: Stereomutation of Pentavalent Compounds: Validating the Berry Pseudorotation, Redressing Ugi’s Turnstile Rotation, and Revealing the Two- and Three-Arm Turnstiles. J Am Chem Soc 2010, 132, 18127. <http://dx.doi.org/10.1021/ja105306s>
• Bartosik Joanna, Mudring Anja-Verena: [Ni(tmen)(acac)][B(Ph)4] a probe for the anion basicity of ionic liquids. Phys Chem Chem Phys 2010, 12, 4005. <http://dx.doi.org/10.1039/b920530f>
• Zech Oliver, Hunger Johannes, Sangoro Joshua R., Iacob Ciprian, Kremer Friedrich, Kunz Werner, Buchner Richard: Correlation between polarity parameters and dielectric properties of [Na][TOTO]—a sodium ionic liquid. Phys Chem Chem Phys 2010, 12, 14341. <http://dx.doi.org/10.1039/c0cp00840k>
• Lange Clifford R., Méndez-Sánchez Noemí: Biological and Abiotic Color Reduction of Paper Mill Effluents during Anaerobic Composting. J Envir Engrg 2010, 136, 701. <http://dx.doi.org/10.1061/(ASCE)EE.1943-7870.0000204>
• Ward Sarah, Messier Tammy, Lukeman Matthew: Electrophilicity of a 9-aryl-9-fluorenyl cation in water — Kinetic evidence for antiaromaticity. Can J Chem 2010, 88, 493. <http://dx.doi.org/10.1139/V10-032>
• Widenhoefer Ross A.: Eine palladiumkatalysierte formale (4+1)-Anellierung: ein neuer Ansatz zum Aufbau von Cyclopentenen. Angew Chem 2009, 121, 7084. <http://dx.doi.org/10.1002/ange.200902404>
• Widenhoefer Ross A.: A Palladium-Catalyzed Formal (4+1) Annulation: A New Approach to Cyclopentene Construction. Angew Chem Int Ed 2009, 48, 6950. <http://dx.doi.org/10.1002/anie.200902404>
• Olivares-Marín M., Del Prete V., Garcia-Moruno E., Fernández-González C., Macías-García A., Gómez-Serrano V.: The development of an activated carbon from cherry stones and its use in the removal of ochratoxin A from red wine. J Food Control 2009, 20, 298. <http://dx.doi.org/10.1016/j.foodcont.2008.05.008>
• Calderazzo Fausto, Masi Francesco, Pampaloni Guido: Homonuclear and heteronuclear transition metal complexes by syn-proportionation reactions. Inorg Chim Ada 2009, 362, 4291. <http://dx.doi.org/10.1016/j.ica.2009.05.053>
• Kubisa Przemysław: Ionic liquids as solvents for polymerization processes—Progress and challenges. Prog Polym Sci 2009, 34, 1333. <http://dx.doi.org/10.1016/j.progpolymsci.2009.09.001>
• McNitt Kristy A., Parimal Kumar, Share Andrew I., Fahrenbach Albert C., Witlicki Edward H., Pink Maren, Bediako D. Kwabena, Plaisier Christina L., Le Nga, Heeringa Lee P.: Reduction of a Redox-Active Ligand Drives Switching in a Cu(I) Pseudorotaxane by a Bimolecular Mechanism. J Am Chem Soc 2009, 131, 1305. <http://dx.doi.org/10.1021/ja8085593>
• Bauer Mirko, Rollberg Anja, Barth Anina, Spange Stefan: Differentiating Between Dipolarity and Polarizability Effects of Solvents Using the Solvatochromism of Barbiturate Dyes. Eur J Org Chem 2008, 2008, 4475. <http://dx.doi.org/10.1002/ejoc.200800355>
• Kaiser Jan, Röckmann Thomas: Correction of mass spectrometric isotope ratio measurements for isobaric isotopologues of O₂, CO, CO₂, N₂O and SO₂. Rapid Commun Mass Spectrom 2008, 22, 3997. <http://dx.doi.org/10.1002/rcm.3821>
• Birsa Lucian M., Asaftei Luliean V.: Solvatochromism of mesoionic iodo(1,3-dithiol-2-ylium-4-yl)phenolates. Monatshefte für Chemie 2008, 139, 1433. <http://dx.doi.org/10.1007/s00706-008-0944-y>
• Paine John B., Pithawalla Yezdi B., Naworal John D.: Carbohydrate pyrolysis mechanisms from isotopic labeling. APPL PYROLYSIS 2008, 82, 10. <http://dx.doi.org/10.1016/j.jaap.2008.01.002>
• Rivera Augusto, Núñez Martín E., Avella Eliseo, Ríos-Motta Jaime: An NMR study of sequential intermediates and collateral products in the conversion of 1,3,6,8-tetraazatricyclo[4.4.1.13,8]dodecane (TATD) to 1,3,6,8-tetraazatricyclo[4.3.1.13,8]undecane (TATU). Tetrahetron Lett 2008, 49, 2154. <http://dx.doi.org/10.1016/j.tetlet.2008.01.091>
• Baidya M., Mayr Herbert: Nucleophilicities and carbon basicities of DBU and DBN. Chem Commun 2008, 1792. <http://dx.doi.org/10.1039/b801811a>
• Hofmann Katja, Schreiter Katja, Seifert Andreas, Rüffer Tobias, Lang Heinrich, Spange Stefan: Solvatochromism and linear solvation energy relationship of diol- and proline-functionalized azo dyes using the Kamlet–Taft and Catalán solvent parameter sets. New J Chem 2008, 32, 2180. <http://dx.doi.org/10.1039/b809055f>
• PATTERSON DOUGLAS: Truth-definitions and Definitional Truth. Midwest Stud Philos 2008, 32, 313. <http://dx.doi.org/10.1111/j.1475-4975.2008.00177.x>
• Kalinin A. A., Isaikina O. G., Mamedov V. A.: Quinoxaline-benzimidazole rearrangements in the reactions of 3-alkanoylquinoxalin-2-ones with 1,2-phenylenediamines. Chem Heterocycl Compd 2007, 43, 1307. <http://dx.doi.org/10.1007/s10593-007-0198-3>
• Paine John B., Pithawalla Yezdi B., Naworal John D., Thomas Charles E.: Carbohydrate pyrolysis mechanisms from isotopic labeling. J Anal App Pyrol 2007, 80, 297. <http://dx.doi.org/10.1016/j.jaap.2007.03.007>
• Caner Hava, Cheeseman James R., Agranat Israel: Conformational spaces of the gastrointestinal antisecretory chiral drug omeprazole: Stereochemistry and tautomerism. Chirality 2006, 18, 10. <http://dx.doi.org/10.1002/chir.20214>
• Reichardt Christian: Polarity of ionic liquids determined empirically by means of solvatochromic pyridinium N-phenolate betaine dyes. Green Chem 2005, 7, 339. <http://dx.doi.org/10.1039/b500106b>
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• Kaiser Jan: Contribution of mass-dependent fractionation to the oxygen isotope anomaly of atmospheric nitrous oxide. J Geophys Res 2004, 109, D03305. <http://dx.doi.org/10.1029/2003JD004088>
• Wallraff G. M., Medeiros D. R., Sanchez M., Petrillo K., Huang W.-S., Rettner C., Davis B., Larson C. E., Sundberg L., Brock P. J.: Sub-50 nm half-pitch imaging with a low activation energy chemically amplified photoresist. JOURNAL OF VACUUM SCIENCE & TECHNOLOGY B 2004, 22, 3479. <http://dx.doi.org/10.1116/1.1813463>
• Birsa Mihail Lucian, Ganju Dumitru: Synthesis and UV/Vis spectroscopic properties of new [2-(N,N-dialkylamino)-1,3-dithiolium-4-yl]phenolates. J Phys Org Chem 2003, 16, 207. <http://dx.doi.org/10.1002/poc.599>
• Reichardt Christian, Röchling Andreas, Schäfer Gerhard: Syntheses and UV-visible spectroscopic properties of two new hydrophilic 2,6-di(carbamoyl)-substituted solvatochromic pyridiniumN-phenolate betaine dyes. J Phys Org Chem 2003, 16, 682. <http://dx.doi.org/10.1002/poc.623>
• Tucker Richard J., Fallis Ian A., Farley Robert D., Murphy Damien M., Willock David J.: An ENDOR and DFT analysis of ‘solvatochromic’ effects in an oxovanadium (IV) complex. chem phys letts 2003, 380, 758. <http://dx.doi.org/10.1016/j.cplett.2003.09.077>
• Sánchez Ignacio E., Kiefhaber Thomas: Non-linear rate-equilibrium free energy relationships and Hammond behavior in protein folding. biophys chem 2003, 100, 397. <http://dx.doi.org/10.1016/S0301-4622(02)00294-6>
• Kaiser Jan: Intramolecular ¹⁵N and ¹⁸O fractionation in the reaction of N₂O with O(¹D) and its implications for the stratospheric N₂O isotope signature. J Geophys Res 2002, 107, 4214. <http://dx.doi.org/10.1029/2001JD001506>
• Goldsmith P. F., Li D., Bergin E. A., Melnick G. J., Tolls V., Howe J. E., Snell R. L., Neufeld D. A.: Tentative Detection of Molecular Oxygen in the ρ Ophiuchi Cloud. astrophys j 2002, 576, 814. <http://dx.doi.org/10.1086/341809>
• Reichardt Christian, Che Daqing, Heckenkemper Guido, Schäfer Gerhard: Syntheses and UV/Vis-Spectroscopic Properties of Hydrophilic 2-, 3-, and 4-Pyridyl-Substituted Solvatochromic and Halochromic PyridiniumN-Phenolate Betaine Dyes as New Empirical Solvent Polarity Indicators. Eur J Org Chem 2001, 2001, 2343. <http://dx.doi.org/10.1002/1099-0690(200106)2001:12<2343::AID-EJOC2343>3.0.CO;2-I>
• Reichardt Christian, Eschner Michael, Schäfer Gerhard: Syntheses and UV-visible spectroscopic properties of new ‘fluorophilic’ fluorine- and perfluoroalkyl-substituted solvatochromic pyridiniumN-phenolate betaine dyes. J Phys Org Chem 2001, 14, 737. <http://dx.doi.org/10.1002/poc.427>
• Vetter Walter: ENANTIOSELECTIVE FATE OF CHIRAL CHLORINATED HYDROCARBONS AND THEIR METABOLITES IN ENVIRONMENTAL SAMPLES. Food Rev Intern 2001, 17, 113. <http://dx.doi.org/10.1081/FRI-100000513>
• Carrea Giacomo, Riva Sergio: Enzyme in organischen Lösungsmitteln: Eigenschaften und Einsatz in der Synthese. Angew Chem 2000, 112, 2312. <http://dx.doi.org/10.1002/1521-3757(20000703)112:13<2312::AID-ANGE2312>3.0.CO;2-4>
• Blomberg Lars G., Wan Hong: Determination of enantiomeric excess by capillary electrophoresis. Eletrophoresis 2000, 21, 1940. <http://dx.doi.org/10.1002/1522-2683(20000601)21:10<1940::AID-ELPS1940>3.0.CO;2-#>
• Karlsson Annika, Broo Anders, Ahlberg Per: Regioselective protonation of ferrocene in superacid and formation of a C—H—Fe bond. An experimental and theoretical study of the structure and dynamics of the ferrocenonium ion. Can J Chem 1999, 77, 628. <http://dx.doi.org/10.1139/v99-053>
• Bennour Sadjia, Toullec Jean: General acid-catalyzed addition of methanol to (E)-N-benzylideneanilines. Can J Chem 1999, 77, 760. <http://dx.doi.org/10.1139/v99-070>
• Reichardt Christian, Löbbecke Stefan, Mehranpour Abdol Mohammed, Schäfer Gerhard: Pyridinium N-phenoxide betaines and their application to the determination of solvent polarities, XXIV. ^{Syntheses and UV-vis spectroscopic properties of new lipophilic tert-butyl- and 1-adamantyl substituted, negatively solvatochromic pyridinium N-phenolate betaine dyes. Can J Chem 1998, 76, 686. <http://dx.doi.org/10.1139/v98-019>}
• Reichardt Christian, Blum Andreas, Harms Klaus, Schäfer Gerhard: PyridiniumN-Phenolate Betaine Dyes and Their Application to the Characterization of the Polarity of Solvents, XXII. Syntheses and UV/Vis Spectroscopic Properties of Solvatochromic, Halochromic, and Chiro-Solvatochromic PyridiniumN-Phenolate Betaine Dyes with Four Stereogenic Centers. Liebigs Ann /Recueil 1997, 1997, 707. <http://dx.doi.org/10.1002/jlac.199719970411>
• Eberhardt Runar, Löbbecke Stefan, Neidhart Bernd, Reichardt Christian: PyridiniumN-Phenoxide Betaines and Their Application to the Characterization of Solvent Polarities, XXIII. Determination ofET(30) Values of Supercritical Carbon Dioxide at Various Pressures and Temperatures. Liebigs Ann /Recueil 1997, 1997, 1195. <http://dx.doi.org/10.1002/jlac.199719970622>
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