Physikalische Chemie Research Articles

Description of Electron Delocalization via the Analysis of Molecular Fields

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDescription of Electron Delocalization via the Analysis of Molecular FieldsGabriel Merino, Alberto Vela, and Thomas HeineView Author Information Institut für Physikalische Chemie und Elektrochemie, TU Dresden, D-01062 Dresden, Germany, and Departamento de Química, Centro de Investigación y de Estudios Avanzados, A. P. 14-740, México, D.F. 07000, México Cite this: Chem. Rev. 2005, 105, 10, 3812–3841Publication Date (Web):September 27, 2005Publication History Received2 December 2004Published online27 September 2005Published inissue 1 October 2005https://doi.org/10.1021/cr030086pCopyright © 2005 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views2001Altmetric-Citations146LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit Read OnlinePDF (2 MB) Get e-AlertsSUBJECTS:Aromatic compounds,Delocalization,Electrical properties,Electron density,Molecules Get e-Alerts

Ultrafast and Low Barrier Motions in the Photoreactions of the Green Fluorescent Protein

Green fluorescent protein (GFP) fluoresces efficiently under blue excitation despite major electrostatic rearrangements resulting from photoionization of the chromophore and neutralization of Glu-222. A competing phototransformation process, which ionizes the chromophore and decarboxylates Glu-222, mimics the electrostatic and structural changes in the fluorescence photocycle. Structural and spectroscopic analysis of the cryogenically stabilized photoproduct at 100 K and a structurally annealed intermediate of the phototransformed protein at 170 K reveals distinct structural relaxations involving protein, chromophore, solvent, and photogenerated CO2. Strong structural changes of the 100 K photoproduct after decarboxylation appear exclusively within 15 angstroms of the chromophore and include the electrostatically driven perturbations of Gln-69, Cys-70, and water molecules in an H-bonding network connecting the chromophore. X-ray crystallography to 1.85 angstroms resolution and static and picosecond time-resolved IR spectroscopy identify structural mechanisms common to phototransformation and to the fluorescence photocycle. In particular, the appearance of a 1697 cm(-1) (+) difference band in both photocycle and phototransformation intermediates is a spectroscopic signature for the structural perturbation of Gln-69. This is taken as evidence for an electrostatically driven dynamic response that is common to both photoreaction pathways. The interactions between the chromophore and the perturbed residues and solvent are decreased or removed in the T203H single and T203H/Q69L double mutants, resulting in a strong reduction of the fluorescence quantum yield. This suggests that the electrostatic response to the transient formation of a buried charge in the wild type is important for the bright fluorescence.

Energy Landscapes. Applications to Clusters, Biomolecules and Glasses. By David J. Wales.

Angewandte Chemie International EditionVolume 44, Issue 12 p. 1756-1757 Book Review Energy Landscapes. Applications to Clusters, Biomolecules and Glasses. By David J. Wales. Andreas Heuer, Andreas Heuer Institut für Physikalische Chemie, Universität Münster, GermanySearch for more papers by this author Andreas Heuer, Andreas Heuer Institut für Physikalische Chemie, Universität Münster, GermanySearch for more papers by this author First published: 08 March 2005 https://doi.org/10.1002/anie.200485197Citations: 2Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume44, Issue12March 11, 2005Pages 1756-1757 RelatedInformation

Energy Landscapes. With Applications to Clusters, Biomolecules and Glasses. Von David J. Wales.

Angewandte ChemieVolume 117, Issue 12 p. 1784-1785 Buchbesprechung Energy Landscapes. With Applications to Clusters, Biomolecules and Glasses. Von David J. Wales. Andreas Heuer, Andreas Heuer Institut für Physikalische Chemie, Universität MünsterSearch for more papers by this author Andreas Heuer, Andreas Heuer Institut für Physikalische Chemie, Universität MünsterSearch for more papers by this author First published: 08 March 2005 https://doi.org/10.1002/ange.200485197Read the full textAboutPDF ToolsRequest permissionAdd to favorites ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume117, Issue12March 11, 2005Pages 1784-1785 This is the German version of Angewandte Chemie. Note for articles published since 1962: Do not cite this version alone. Take me to the International Edition version with citable page numbers, DOI, and citation export. We apologize for the inconvenience. RelatedInformation

A 3D-NMR Method for Studying Hydrocarbon-Based Polymer Structures

ADVERTISEMENT RETURN TO ISSUEPREVCommunication to the...Communication to the EditorNEXTA 3D-NMR Method for Studying Hydrocarbon-Based Polymer StructuresMasud Monwar, Sangrama K. Sahoo, Peter L. Rinaldi, Elizabeth F. McCord, Donald R. Marshall, Michael Buback, and Henning LatzView Author Information Department of Chemistry, University of Akron, Akron, Ohio 44325-3601 Dupont Experimental Station, Bldg 328, Rm 133, Route 141 and Powder Mill Rd., Wilmington, Delaware 19880-328 Institut für Physikalische Chemie, Universität Göttingen, Tammannstr. 6, D 37077 Göttingen, Germany Cite this: Macromolecules 2003, 36, 18, 6695–6697Publication Date (Web):August 14, 2003Publication History Received27 May 2003Published online14 August 2003Published inissue 1 September 2003https://doi.org/10.1021/ma030292zCopyright © 2003 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views168Altmetric-Citations5LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit Read OnlinePDF (70 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Carbon,Carbonyls,Chemical structure,Nuclear magnetic resonance spectroscopy,Polymers Get e-Alerts

Book Review: Metal Oxygen Clusters. The Surface and Catalytic Properties of Heteropoly Oxometalates. By John B. Moffat

Angewandte Chemie International EditionVolume 41, Issue 14 p. 2611-2611 Book Review Book Review: Metal Oxygen Clusters. The Surface and Catalytic Properties of Heteropoly Oxometalates. By John B. Moffat Helmut Knözinger, Helmut Knözinger Department Chemie Physikalische Chemie Universität München Munich (Germany)Search for more papers by this author Helmut Knözinger, Helmut Knözinger Department Chemie Physikalische Chemie Universität München Munich (Germany)Search for more papers by this author First published: 15 July 2002 https://doi.org/10.1002/1521-3773(20020715)41:14<2611::AID-ANIE2611>3.0.CO;2-7Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume41, Issue14July 15, 2002Pages 2611-2611 RelatedInformation

Buchbesprechung: Metal Oxygen Clusters. The Surface and Catalytic Properties of Heteropoly Oxometalates. Von John B.Moffat

Angewandte ChemieVolume 114, Issue 14 p. 2725-2725 Buchbesprechung Buchbesprechung: Metal Oxygen Clusters. The Surface and Catalytic Properties of Heteropoly Oxometalates. Von John B.Moffat Helmut Knözinger, Helmut Knözinger Department Chemie/ Physikalische Chemie der Universität München (Germany)Search for more papers by this author Helmut Knözinger, Helmut Knözinger Department Chemie/ Physikalische Chemie der Universität München (Germany)Search for more papers by this author First published: 15 July 2002 https://doi.org/10.1002/1521-3757(20020715)114:14<2725::AID-ANGE11112725>3.0.CO;2-6Read the full textAboutPDF ToolsRequest permissionAdd to favorites ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume114, Issue14July 15, 2002Pages 2725-2725 This is the German version of Angewandte Chemie. Note for articles published since 1962: Do not cite this version alone. Take me to the International Edition version with citable page numbers, DOI, and citation export. We apologize for the inconvenience. RelatedInformation

Quadruple hydrogen bonds of ureido-pyrimidinone moieties investigated in the solid state by 1H double-quantum MAS NMR spectroscopyPresented as part of a plenary lecture by H. W. Spiess at the annual meeting of the Deutsche Bunsen-Gesellschaft für Physikalische Chemie, Potsdam, May 9–11, 2002.

The structure of the quadruple hydrogen bond formed by ureido-pyrimidinone moieties is investigated in dimerised model compounds, as well as in a supramolecular polymer, by solid-state 1H double-quantum (DQ) NMR spectroscopy under fast magic-angle spinning (MAS). This NMR method combines the sensitivity of 1H NMR chemical shifts to the strengths of hydrogen bonds with quantitative information about dipole–dipole couplings between pairs of protons. Thus, two-dimensional 1H DQ MAS spectra provide particularly detailed insight into the arrangement of hydrogen bonds and allow proton–proton distances to be measured. For the supramolecular polymer, a thermally induced irreversible tautomeric rearrangement of the hydrogen-bonded moieties is elucidated in the bulk material. This process is associated with an Arrhenius activation energy of (145 ± 15) kJ mol−1, which can be rationalised in terms of hydrogen-bond dissociation and the reorientation of the supramolecular polymer chain.

Fluid phase diagrams of ternary systems with one volatile component and immiscibility in two of the constituent binary mixturesPresented at the International Bunsen Discussion Meeting of the Deutsche Bunsen-Gesellschaft für Physikalische Chemie, Walberberg, Germany, 19–22 August, 2001.

Four types of fluid phase diagram where the critical curves and immiscibility regions are not intersected by crystallization surfaces are selected as the main types of fluid phase behavior in binary mixtures. These types are used as a starting point for the systematic classification of the main types of binary complete phase diagram, describing any equilibria with liquid, gas and solid phases over a wide range of temperatures and pressures, by the method of continuous topological transformation. This method and the classification of binary phase diagrams, containing the boundary version phase diagrams with ternary nonvariant points, are used as a quasi-binary approach to derive the main types of fluid phase behavior for ternary mixtures with one volatile component and immiscibility in two of the constituent binary subsystems. In such ternary systems there are six classes distinguished by the types of fluid phase behavior in the binary subsystems. A wide variety of ternary fluid phase diagrams, obtained either by a transformation of the topological types or by changing the location of nonvariant points without transformation of topological types, is discussed.

Per‐Olov Löwdin curriculum vitae

Per‐Olov Löwdin curriculum vitae

Call for papers: Special issue on “Molecular physics of building blocks of life under isolated or defined conditions”

Submission until end of 2001 Scheduled for publication in Sept./Oct. 2002 The new research field studying “Building blocks of life under isolated or defined conditions” is showing rapid growth. New technical and experimental developments have stimulated recent progress in the investigation of biologically relevant, but thermally unstable, molecules in well defined environments. At the same time, enormous progress in computer power and the development of more efficient computational methods now make it possible to calculate large, flexible systems, such as small peptides and nucleobase pairs, at unprecedented levels of theory. While this approach does not claim to try and understand biological systems in situ, it does aim to explore their detailed intramolecular properties, otherwise hidden in the averaging of states, structures, conformers and sites, inherent in the solution phase and under other undefined conditions.[-2.5mm] Special conditions, such as low temperatures, defined environments or the observation of isolated and selected or even single molecules, can generate high resolution data which, combined with theory, can provide fundamental insights into the detailed properties of biomolecules. This approach reveals their dipole moments, ionization energies, electron affinities, proton affinities, structural shape, electronic structure, photodynamics and reactivity, but also their structural arrangement and binding strength to themselfs, to other building blocks of life or to solvent molecules.[-2.5mm] Our focus for this special issue is on the most fundamental biomolecular building blocks, including, but not limited to nucleic acid bases, nucleotides, amino acids and small as well as large peptides or proteins and complexes thereof. Investigations may include, for example, rotationally, vibrationally and electronically resolved spectroscopy with different excitation schemes, such as multiphoton ionization, laser induced fluorescence, photodissociation, photoelectron spectroscopy techniques and variety of mass spectrometric methods, such as ion-drift and ICR based approaches. New double resonance techniques allow assignments of conformer, isomer and tautomer structures which often coexist in molecules and complexes of biological interest. A great advantage of specific and detailed experimental results under well-defined conditions is the possibility of direct comparisons with theoretical calculations. This makes it possible to explore the shape of the potential energy surface, atomic charge densities, and contributions of individual forces to binding energies and solvation. We invite all molecular physicists, chemists and biochemists, experimentalists and theoreticians alike, who study molecular systems of biological interest under well defined conditions, to contribute to this special issue. Please send your manuscripts to the EPJ Editorial Office, Universite Paris-Sud, Bâtiment 510, F-91405 Orsay Cedex, France or to one of the guest editors below Karl Kleinermanns Heinrich-Heine-Universitat Dusseldorf Institut fur Physikalische Chemie I Universitatsstrase 1 40225 Dusseldorf – Germany Tel. (49) 211 811 3691 – Fax: (49) 211 811 5195 e-mail: kleinermanns@uni-duesseldorf.de Jean-Pierre Schermann Universite Paris-Nord Institut Galilee Laboratoire de Physique des Lasers 93430 Villetaneuse – France Tel. (33) 1 4940 3816 – Fax. (33) 1 4940 3200 e-mail: schermann@lpl.univ-paris13.fr Mattanjah S. de Vries Department of Chemistry and Biochemistry University of California Santa Barbara, CA 93106 – USA Tel: (805) 893-5921 – Fax: (805) 893-4120 e-mail: devries@chem.ucsb.edu Dr. Rainer Weinkauf Heinrich-Heine-Universitat Dusseldorf Institut fur Physikalische Chemie I Universitatsstrase 1 40225 Dusseldorf – Germany Tel. (49) 211 81 11729 – Fax: (49) 211 81 11730 e-mail: weinkauf@uni-duesseldorf.de For a faster assessment electronic submission is highly encouraged (e-mail: epjd@edpsciences.org). Instruction for preparing the manuscripts are given at http://www.edpsciences.org Karl Kleinermanns, Jean-Pierre Schermann, Mattanjah S. de Vries, Rainer Weinkauf

Nanorainbows: graded semiconductor films from quantum dots.

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTNanorainbows: Graded Semiconductor Films from Quantum DotsArif A. Mamedov, Artem Belov, Michael Giersig, Nataliya N. Mamedova, and Nicholas A. KotovView Author Information ChemistryDepartment, Oklahoma State University Stillwater, Oklahoma, 74078 Hahn-Meitner-Institut, Abteilung Physikalische Chemie Glienickerstrasse 100, D-15109, Berlin, Germany Cite this: J. Am. Chem. Soc. 2001, 123, 31, 7738–7739Publication Date (Web):July 17, 2001Publication History Received21 March 2001Revised20 May 2001Published online17 July 2001Published inissue 1 August 2001https://doi.org/10.1021/ja015857qCopyright © 2001 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views2038Altmetric-Citations265LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit Read OnlinePDF (92 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Deposition,Layers,Luminescence,Polyelectrolytes,Thin films Get e-Alerts

Charge-Induced Partial Ordering of Boron around Structure Directing Agents in Zeolites Observed by 13C{11B} Rotational Echo Double Resonance NMR

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTCharge-Induced Partial Ordering of Boron around Structure Directing Agents in Zeolites Observed by 13C{11B} Rotational Echo Double Resonance NMRChristian Fild, Hellmut Eckert, and Hubert KollerView Author Information Institut für Physikalische Chemie Westfälische Wilhelms-Universität Münster Schlossplatz 4/7, D-48149 Münster, Germany Cite this: J. Am. Chem. Soc. 2000, 122, 50, 12590–12591Publication Date (Web):November 30, 2000Publication History Received14 September 2000Published online30 November 2000Published inissue 1 December 2000https://doi.org/10.1021/ja005609eCopyright © 2000 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views188Altmetric-Citations14LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit Read OnlinePDF (37 KB) Get e-AlertsSUBJECTS:Boron,Lattices,Molecular structure,Nuclear magnetic resonance spectroscopy,Zeolites Get e-Alerts

Surface-Enhanced Raman Scattering Spectroscopy of Single Carbon Domains on Individual Ag Nanoparticles on a 25 ms Time Scale

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTSurface-Enhanced Raman Scattering Spectroscopy of Single Carbon Domains on Individual Ag Nanoparticles on a 25 ms Time ScalePatrick J. Moyer, Jan Schmidt, Lukas M. Eng, Alfred J. Meixner, Gunther W. Sandmann, Hartmut Dietz, and Waldfried PliethView Author Information Institut für Angewandte Photophysik Technische Universität, 01062 Dresden, Germany Institut für Physikalische Chemie und Elektrochemie Technische Universität, 01062 Dresden, Germany Cite this: J. Am. Chem. Soc. 2000, 122, 22, 5409–5410Publication Date (Web):May 18, 2000Publication History Received28 February 2000Published online18 May 2000Published inissue 1 June 2000https://doi.org/10.1021/ja000703gCopyright © 2000 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views833Altmetric-Citations72LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit Read OnlinePDF (82 KB) Get e-AlertsSUBJECTS:Anode materials,Carbon,Metal nanoparticles,Nanoparticles,Raman spectroscopy Get e-Alerts

Reversible Cell Aggregation Induced by Specific Ligand−Receptor Coupling

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTReversible Cell Aggregation Induced by Specific Ligand−Receptor CouplingWolfgang MeierView Author Information Institut für Physikalische Chemie, Departement Chemie, Universität Basel, Klingelbergstrasse 80, CH-4056 Basel, Switzerland Cite this: Langmuir 2000, 16, 3, 1457–1459Publication Date (Web):November 4, 1999Publication History Received12 July 1999Revised27 September 1999Published online4 November 1999Published inissue 1 February 2000https://doi.org/10.1021/la990915vCopyright © 2000 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views204Altmetric-Citations19LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit Read OnlinePDF (162 KB) Get e-AlertsSUBJECTS:Hydrophobicity,Membranes,Nutrition,Organic compounds,Polymers Get e-Alerts

Nonclassical, Cyclically Delocalized 4N/3e Radical Cations and 4N/2e Dications: One- and Two-Electron Oxidation of Proximate, syn-Periplanar Bisdiazene-Oxides

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTNonclassical, Cyclically Delocalized 4N/3e Radical Cations and 4N/2e Dications: One- and Two-Electron Oxidation of Proximate, syn-Periplanar Bisdiazene-OxidesKai Exner, Horst Prinzbach, Georg Gescheidt, Birgit Grossmann, and Jürgen HeinzeView Author Information Institut für Organische Chemie und Biochemie der Universität, Albertstrasse 21 D-79104 Freiburg, Germany Institut für Physikalische Chemie der Universität Klingelbergstrasse 80, CH-4056 Basel, Schweiz Institut für Physikalische Chemie der Universität Albertstrasse 21, D-79104 Freiburg, Germany Cite this: J. Am. Chem. Soc. 1999, 121, 9, 1964–1965Publication Date (Web):February 19, 1999Publication History Received28 October 1998Published online19 February 1999Published inissue 1 March 1999https://doi.org/10.1021/ja9837607Copyright © 1999 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views111Altmetric-Citations17LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit Read OnlinePDF (81 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Cations,Electron paramagnetic resonance spectroscopy,Organic compounds,Oxidation,Redox reactions Get e-Alerts

Dielectric Properties of Some Ethoxylated Primary Amines in Nonaqueous Medium. Effect of Added Alcohol on Dipole Moment and CMC Values

Article Dielectric Properties of Some Ethoxylated Primary Amines in Nonaqueous Medium. Effect of Added Alcohol on Dipole Moment and CMC Values was published on February 1, 1999 in the journal Zeitschrift für Physikalische Chemie (volume 211, issue 2).

Type B Semiconductor Photocatalysis: On the Mechanism of the CdS-Catalyzed Linear Photoaddition of 2,5-Dihydrofuran to Azobenzene

Article Type B Semiconductor Photocatalysis: On the Mechanism of the CdS-Catalyzed Linear Photoaddition of 2,5-Dihydrofuran to Azobenzene was published on February 1, 1999 in the journal Zeitschrift für Physikalische Chemie (volume 213, issue 2).

Nanoparticles and Nanostructured Films, Preparation, Characterization and Applications

Article Nanoparticles and Nanostructured Films, Preparation, Characterization and Applications was published on February 1, 1999 in the journal Zeitschrift für Physikalische Chemie (volume 213, issue 2).

Raman- and Infrared Spectroscopic Investigation of Aqueous ZnSO4 Solutions from 8°C to 165°C: Inner- and Outer-Sphere Complexes

Article Raman- and Infrared Spectroscopic Investigation of Aqueous ZnSO4 Solutions from 8°C to 165°C: Inner- and Outer-Sphere Complexes was published on February 1, 1999 in the journal Zeitschrift für Physikalische Chemie (volume 209, issue 2).