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Biblioteca

MARC Lista (tabellare)
Advances in physical organic chemistry . Volume 45 / / editor, John P. Richard
Advances in physical organic chemistry . Volume 45 / / editor, John P. Richard
Edizione [1st ed.]
Pubbl/distr/stampa Oxford, : Academic Press, an imprint of Elsevier, 2011
Descrizione fisica 1 online resource (273 p.)
Disciplina 547.13
547.30877
Altri autori (Persone) RichardJ. P (John P.)
Collana Advances in physical organic chemistry
Soggetto topico Physical organic chemistry
ISBN 1-283-27599-6
9786613275998
0-12-386048-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front cover; Advances in Physical Organic Chemistry; Copyright; Contents; Author Index; Cumulative Index of Authors; Cumulative Index of Titles; Subject Index
Record Nr. UNINA-9910163948403321
Oxford, : Academic Press, an imprint of Elsevier, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Brownian Motion : Elements of Colloid Dynamics / / by Albert P. Philipse
Brownian Motion : Elements of Colloid Dynamics / / by Albert P. Philipse
Autore Philipse Albert P
Edizione [1st ed. 2018.]
Pubbl/distr/stampa Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018
Descrizione fisica 1 online resource (XVII, 178 p. 50 illus., 15 illus. in color.)
Disciplina 547.13
Collana Undergraduate Lecture Notes in Physics
Soggetto topico Amorphous substances
Complex fluids
Physical chemistry
Thermodynamics
Fluids
Soft and Granular Matter, Complex Fluids and Microfluidics
Physical Chemistry
Fluid- and Aerodynamics
ISBN 3-319-98053-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preface -- A first round of Brownian motion -- The feverish Sphinx -- Kinetic theory.-. A tale of ten time scales.-Continuity, constitution and Fick’s laws -- Brownian displacements -- Fluid flow -- Flow past spheres and simple geometries -- Encounters of the Brownian kind -- Randon walks in external fields -- Brownian motion and Van 't Hoff's law- Appendices: A. Moments, fluctuations and Gaussian integrals -- B. Summary vector calculus -- C. Answers to selected problems -- Index -- Greek/Roman symbols. .
Record Nr. UNINA-9910300161103321
Philipse Albert P  
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Chemometric methods in molecular design [[electronic resource] /] / edited by Han van de Waterbeemd
Chemometric methods in molecular design [[electronic resource] /] / edited by Han van de Waterbeemd
Pubbl/distr/stampa Weinheim, Ger. ; ; New York, : VCH, c1995
Descrizione fisica 1 online resource (380 p.)
Disciplina 547.13
615/.1901
Altri autori (Persone) WaterbeemdHan van de
Collana Methods and principles in medicinal chemistry
Soggetto topico QSAR (Biochemistry)
Drugs - Design
Soggetto genere / forma Electronic books.
ISBN 1-281-75866-3
9786611758660
3-527-61545-8
3-527-61544-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chernornetric Methods in Molecular Design; Preface; A Personal Foreword; Contents; 1 Introduction; 1.1 Quantitative Molecular Design; 1.2 Chemometrics; 1.3 The Hansch Approach; 1.4 Modern Chemometric Approaches in Molecular Design; 1.5 Software; 1.5.1 General Statistical Packages; 1.5.2 Specialized Software for SPC Studies; References; 2 Molecular Concepts; 2.1 Representations of Molecules; 2.1.1 Introduction; 2.1.2 Substituent Constants; 2.1.2.1 Electronic Substituent Constants; 2.1.2.2 The Hydrophobic Substituent Constant,p; 2.1.2.3 Partition Coefficient - Log P
2.1.2.4 Steric Substituent Constants2.1.3 Whole Molecule Representations; 2.1.3.1 Topological Descriptions; 2.1.3.2 Electronic Whole Molecule Descriptors; 2.1.3.3 Geometric Descriptors; References; 2.2 Atom-Level Descriptors for QSAR Analyzes; 2.2.1 Introduction; 2.2.2 An Atom-Level Description of Structure; 2.2.2.1 The Field; 2.2.2.2 The Intrinsic State of an Atom; 2.2.2.3 The Field Effect on Each Atom; 2.2.3 Strategies for Use of E-State Indices; 2.2.4 Examples of E-State QSAR; 2.2.4.1 MAO Inhibition with Hydrazides; 2.2.4.2 Adenosine A, Inhibitors
2.2.4.3 Anesthetic Concentration of Haloalkanes2.2.4.4 Odor Sensitivity of Pyrazines; 2.2.5 Conclusions; References; 3 Experimental Design in Synthesis Planning and Structure-Property Correlations; 3.1 Experimental Design; 3.1.1 The Importance of Experimental Design in Medicinal Chemistry; 3.1.2 Strategy in Experimental Design; 3.1.3 Selected Methods for Experimental Design; 3.1.3.1 Methods for the Direct Optimization of Lead Compounds; 3.1.3.2 Methods for the Systematic Investigation of Parameter Space; 3.1.3.3 Choice of Molecular Descriptors; 3.1.4 Summary and Conclusion; References
3.2 Applications of Statistical Experimental Design and PLS Modeling in QSAR3.2.1 Introduction; 3.2.2 A Strategy for QSAR Development in Drug Design; 3.2.2.1 Formulation of Classes of Similar Compounds (Step 1); 3.2.2.2 Structural Description and Definition of Design Variables (Step 2); 3.2.2.3 Selection of the Training Set of Compounds (Step 3); 3.2.2.4 Biological Testing (Step 4); 3.2.2.5 QSAR Development (Step 5; 3.2.2.6 Validation and Predictions for Non-Tested Compounds (Step; 3.2.3 Examples of Design and PLS Modeling; 3.2.3.1 Bradykinin Potentiating Pentapeptides
3.2.3.2 Dipeptides (Inhibiting the Angiotensin Converting Enzyme)3.2.3.3 Dipeptides (Bitter Tasting); 3.2.3.4 Mimetics; 3.2.3.5 Haloalkanes; 3.2.3.6 Dibenzofurans; 3.2.3.7 Monosubstituted Benzenes; 3.2.3.8 Corrosive Carboxylic Acids; 3.2.4 Discussion and Conclusions; Software Used; Acknowledgements; References; 3.3 Total Response Surface Optimization; 3.3.1 Background; 3.3.2 Representation of a Response Surface; 3.3.3 Structure Descriptors from Chemical Graph Theory; 3.3.4 Examples; 3.3.4.1 Neurotoxicity of Fluorophosphorous Compounds
3.3.4.2 Bioconcentration of Chlorinated Phenyls and Biphenyls
Record Nr. UNINA-9910144132703321
Weinheim, Ger. ; ; New York, : VCH, c1995
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chemometric methods in molecular design [[electronic resource] /] / edited by Han van de Waterbeemd
Chemometric methods in molecular design [[electronic resource] /] / edited by Han van de Waterbeemd
Pubbl/distr/stampa Weinheim, Ger. ; ; New York, : VCH, c1995
Descrizione fisica 1 online resource (380 p.)
Disciplina 547.13
615/.1901
Altri autori (Persone) WaterbeemdHan van de
Collana Methods and principles in medicinal chemistry
Soggetto topico QSAR (Biochemistry)
Drugs - Design
ISBN 1-281-75866-3
9786611758660
3-527-61545-8
3-527-61544-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chernornetric Methods in Molecular Design; Preface; A Personal Foreword; Contents; 1 Introduction; 1.1 Quantitative Molecular Design; 1.2 Chemometrics; 1.3 The Hansch Approach; 1.4 Modern Chemometric Approaches in Molecular Design; 1.5 Software; 1.5.1 General Statistical Packages; 1.5.2 Specialized Software for SPC Studies; References; 2 Molecular Concepts; 2.1 Representations of Molecules; 2.1.1 Introduction; 2.1.2 Substituent Constants; 2.1.2.1 Electronic Substituent Constants; 2.1.2.2 The Hydrophobic Substituent Constant,p; 2.1.2.3 Partition Coefficient - Log P
2.1.2.4 Steric Substituent Constants2.1.3 Whole Molecule Representations; 2.1.3.1 Topological Descriptions; 2.1.3.2 Electronic Whole Molecule Descriptors; 2.1.3.3 Geometric Descriptors; References; 2.2 Atom-Level Descriptors for QSAR Analyzes; 2.2.1 Introduction; 2.2.2 An Atom-Level Description of Structure; 2.2.2.1 The Field; 2.2.2.2 The Intrinsic State of an Atom; 2.2.2.3 The Field Effect on Each Atom; 2.2.3 Strategies for Use of E-State Indices; 2.2.4 Examples of E-State QSAR; 2.2.4.1 MAO Inhibition with Hydrazides; 2.2.4.2 Adenosine A, Inhibitors
2.2.4.3 Anesthetic Concentration of Haloalkanes2.2.4.4 Odor Sensitivity of Pyrazines; 2.2.5 Conclusions; References; 3 Experimental Design in Synthesis Planning and Structure-Property Correlations; 3.1 Experimental Design; 3.1.1 The Importance of Experimental Design in Medicinal Chemistry; 3.1.2 Strategy in Experimental Design; 3.1.3 Selected Methods for Experimental Design; 3.1.3.1 Methods for the Direct Optimization of Lead Compounds; 3.1.3.2 Methods for the Systematic Investigation of Parameter Space; 3.1.3.3 Choice of Molecular Descriptors; 3.1.4 Summary and Conclusion; References
3.2 Applications of Statistical Experimental Design and PLS Modeling in QSAR3.2.1 Introduction; 3.2.2 A Strategy for QSAR Development in Drug Design; 3.2.2.1 Formulation of Classes of Similar Compounds (Step 1); 3.2.2.2 Structural Description and Definition of Design Variables (Step 2); 3.2.2.3 Selection of the Training Set of Compounds (Step 3); 3.2.2.4 Biological Testing (Step 4); 3.2.2.5 QSAR Development (Step 5; 3.2.2.6 Validation and Predictions for Non-Tested Compounds (Step; 3.2.3 Examples of Design and PLS Modeling; 3.2.3.1 Bradykinin Potentiating Pentapeptides
3.2.3.2 Dipeptides (Inhibiting the Angiotensin Converting Enzyme)3.2.3.3 Dipeptides (Bitter Tasting); 3.2.3.4 Mimetics; 3.2.3.5 Haloalkanes; 3.2.3.6 Dibenzofurans; 3.2.3.7 Monosubstituted Benzenes; 3.2.3.8 Corrosive Carboxylic Acids; 3.2.4 Discussion and Conclusions; Software Used; Acknowledgements; References; 3.3 Total Response Surface Optimization; 3.3.1 Background; 3.3.2 Representation of a Response Surface; 3.3.3 Structure Descriptors from Chemical Graph Theory; 3.3.4 Examples; 3.3.4.1 Neurotoxicity of Fluorophosphorous Compounds
3.3.4.2 Bioconcentration of Chlorinated Phenyls and Biphenyls
Record Nr. UNISA-996218390503316
Weinheim, Ger. ; ; New York, : VCH, c1995
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Chemometric methods in molecular design [[electronic resource] /] / edited by Han van de Waterbeemd
Chemometric methods in molecular design [[electronic resource] /] / edited by Han van de Waterbeemd
Pubbl/distr/stampa Weinheim, Ger. ; ; New York, : VCH, c1995
Descrizione fisica 1 online resource (380 p.)
Disciplina 547.13
615/.1901
Altri autori (Persone) WaterbeemdHan van de
Collana Methods and principles in medicinal chemistry
Soggetto topico QSAR (Biochemistry)
Drugs - Design
ISBN 1-281-75866-3
9786611758660
3-527-61545-8
3-527-61544-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chernornetric Methods in Molecular Design; Preface; A Personal Foreword; Contents; 1 Introduction; 1.1 Quantitative Molecular Design; 1.2 Chemometrics; 1.3 The Hansch Approach; 1.4 Modern Chemometric Approaches in Molecular Design; 1.5 Software; 1.5.1 General Statistical Packages; 1.5.2 Specialized Software for SPC Studies; References; 2 Molecular Concepts; 2.1 Representations of Molecules; 2.1.1 Introduction; 2.1.2 Substituent Constants; 2.1.2.1 Electronic Substituent Constants; 2.1.2.2 The Hydrophobic Substituent Constant,p; 2.1.2.3 Partition Coefficient - Log P
2.1.2.4 Steric Substituent Constants2.1.3 Whole Molecule Representations; 2.1.3.1 Topological Descriptions; 2.1.3.2 Electronic Whole Molecule Descriptors; 2.1.3.3 Geometric Descriptors; References; 2.2 Atom-Level Descriptors for QSAR Analyzes; 2.2.1 Introduction; 2.2.2 An Atom-Level Description of Structure; 2.2.2.1 The Field; 2.2.2.2 The Intrinsic State of an Atom; 2.2.2.3 The Field Effect on Each Atom; 2.2.3 Strategies for Use of E-State Indices; 2.2.4 Examples of E-State QSAR; 2.2.4.1 MAO Inhibition with Hydrazides; 2.2.4.2 Adenosine A, Inhibitors
2.2.4.3 Anesthetic Concentration of Haloalkanes2.2.4.4 Odor Sensitivity of Pyrazines; 2.2.5 Conclusions; References; 3 Experimental Design in Synthesis Planning and Structure-Property Correlations; 3.1 Experimental Design; 3.1.1 The Importance of Experimental Design in Medicinal Chemistry; 3.1.2 Strategy in Experimental Design; 3.1.3 Selected Methods for Experimental Design; 3.1.3.1 Methods for the Direct Optimization of Lead Compounds; 3.1.3.2 Methods for the Systematic Investigation of Parameter Space; 3.1.3.3 Choice of Molecular Descriptors; 3.1.4 Summary and Conclusion; References
3.2 Applications of Statistical Experimental Design and PLS Modeling in QSAR3.2.1 Introduction; 3.2.2 A Strategy for QSAR Development in Drug Design; 3.2.2.1 Formulation of Classes of Similar Compounds (Step 1); 3.2.2.2 Structural Description and Definition of Design Variables (Step 2); 3.2.2.3 Selection of the Training Set of Compounds (Step 3); 3.2.2.4 Biological Testing (Step 4); 3.2.2.5 QSAR Development (Step 5; 3.2.2.6 Validation and Predictions for Non-Tested Compounds (Step; 3.2.3 Examples of Design and PLS Modeling; 3.2.3.1 Bradykinin Potentiating Pentapeptides
3.2.3.2 Dipeptides (Inhibiting the Angiotensin Converting Enzyme)3.2.3.3 Dipeptides (Bitter Tasting); 3.2.3.4 Mimetics; 3.2.3.5 Haloalkanes; 3.2.3.6 Dibenzofurans; 3.2.3.7 Monosubstituted Benzenes; 3.2.3.8 Corrosive Carboxylic Acids; 3.2.4 Discussion and Conclusions; Software Used; Acknowledgements; References; 3.3 Total Response Surface Optimization; 3.3.1 Background; 3.3.2 Representation of a Response Surface; 3.3.3 Structure Descriptors from Chemical Graph Theory; 3.3.4 Examples; 3.3.4.1 Neurotoxicity of Fluorophosphorous Compounds
3.3.4.2 Bioconcentration of Chlorinated Phenyls and Biphenyls
Record Nr. UNINA-9910830975303321
Weinheim, Ger. ; ; New York, : VCH, c1995
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chemometric methods in molecular design / / edited by Han van de Waterbeemd
Chemometric methods in molecular design / / edited by Han van de Waterbeemd
Pubbl/distr/stampa Weinheim, Ger. ; ; New York, : VCH, c1995
Descrizione fisica 1 online resource (380 p.)
Disciplina 547.13
615/.1901
Altri autori (Persone) WaterbeemdHan van de
Collana Methods and principles in medicinal chemistry
Soggetto topico QSAR (Biochemistry)
Drugs - Design
ISBN 9786611758660
9781281758668
1281758663
9783527615452
3527615458
9783527615445
352761544X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chernornetric Methods in Molecular Design; Preface; A Personal Foreword; Contents; 1 Introduction; 1.1 Quantitative Molecular Design; 1.2 Chemometrics; 1.3 The Hansch Approach; 1.4 Modern Chemometric Approaches in Molecular Design; 1.5 Software; 1.5.1 General Statistical Packages; 1.5.2 Specialized Software for SPC Studies; References; 2 Molecular Concepts; 2.1 Representations of Molecules; 2.1.1 Introduction; 2.1.2 Substituent Constants; 2.1.2.1 Electronic Substituent Constants; 2.1.2.2 The Hydrophobic Substituent Constant,p; 2.1.2.3 Partition Coefficient - Log P
2.1.2.4 Steric Substituent Constants2.1.3 Whole Molecule Representations; 2.1.3.1 Topological Descriptions; 2.1.3.2 Electronic Whole Molecule Descriptors; 2.1.3.3 Geometric Descriptors; References; 2.2 Atom-Level Descriptors for QSAR Analyzes; 2.2.1 Introduction; 2.2.2 An Atom-Level Description of Structure; 2.2.2.1 The Field; 2.2.2.2 The Intrinsic State of an Atom; 2.2.2.3 The Field Effect on Each Atom; 2.2.3 Strategies for Use of E-State Indices; 2.2.4 Examples of E-State QSAR; 2.2.4.1 MAO Inhibition with Hydrazides; 2.2.4.2 Adenosine A, Inhibitors
2.2.4.3 Anesthetic Concentration of Haloalkanes2.2.4.4 Odor Sensitivity of Pyrazines; 2.2.5 Conclusions; References; 3 Experimental Design in Synthesis Planning and Structure-Property Correlations; 3.1 Experimental Design; 3.1.1 The Importance of Experimental Design in Medicinal Chemistry; 3.1.2 Strategy in Experimental Design; 3.1.3 Selected Methods for Experimental Design; 3.1.3.1 Methods for the Direct Optimization of Lead Compounds; 3.1.3.2 Methods for the Systematic Investigation of Parameter Space; 3.1.3.3 Choice of Molecular Descriptors; 3.1.4 Summary and Conclusion; References
3.2 Applications of Statistical Experimental Design and PLS Modeling in QSAR3.2.1 Introduction; 3.2.2 A Strategy for QSAR Development in Drug Design; 3.2.2.1 Formulation of Classes of Similar Compounds (Step 1); 3.2.2.2 Structural Description and Definition of Design Variables (Step 2); 3.2.2.3 Selection of the Training Set of Compounds (Step 3); 3.2.2.4 Biological Testing (Step 4); 3.2.2.5 QSAR Development (Step 5; 3.2.2.6 Validation and Predictions for Non-Tested Compounds (Step; 3.2.3 Examples of Design and PLS Modeling; 3.2.3.1 Bradykinin Potentiating Pentapeptides
3.2.3.2 Dipeptides (Inhibiting the Angiotensin Converting Enzyme)3.2.3.3 Dipeptides (Bitter Tasting); 3.2.3.4 Mimetics; 3.2.3.5 Haloalkanes; 3.2.3.6 Dibenzofurans; 3.2.3.7 Monosubstituted Benzenes; 3.2.3.8 Corrosive Carboxylic Acids; 3.2.4 Discussion and Conclusions; Software Used; Acknowledgements; References; 3.3 Total Response Surface Optimization; 3.3.1 Background; 3.3.2 Representation of a Response Surface; 3.3.3 Structure Descriptors from Chemical Graph Theory; 3.3.4 Examples; 3.3.4.1 Neurotoxicity of Fluorophosphorous Compounds
3.3.4.2 Bioconcentration of Chlorinated Phenyls and Biphenyls
Record Nr. UNINA-9910877629303321
Weinheim, Ger. ; ; New York, : VCH, c1995
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chimie des colloides organiques / Hermann Staudinger ; traduit par Henri Gibello
Chimie des colloides organiques / Hermann Staudinger ; traduit par Henri Gibello
Autore Staudinger, Hermann
Pubbl/distr/stampa Paris, : Dunod, 1953
Descrizione fisica XIV, 347 p. : ill. ; 22 cm
Disciplina 547.13
Soggetto non controllato Colloidi organici
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione fre
Record Nr. UNINA-990000024950403321
Staudinger, Hermann  
Paris, : Dunod, 1953
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chimie des colloides...Staudinger, Hermann
Deep eutectic solvents : properties, and applications / / edited by Diego J. Ramon and Gabriela Guillena
Deep eutectic solvents : properties, and applications / / edited by Diego J. Ramon and Gabriela Guillena
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , [2020]
Descrizione fisica 1 online resource (387 pages)
Disciplina 547.13
Soggetto topico Physical organic chemistry
Green chemistry
Soggetto genere / forma Electronic books.
ISBN 3-527-81849-9
3-527-81848-0
3-527-81847-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910555121503321
Weinheim, Germany : , : Wiley-VCH, , [2020]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Deep eutectic solvents : properties, and applications / / edited by Diego J. Ramon and Gabriela Guillena
Deep eutectic solvents : properties, and applications / / edited by Diego J. Ramon and Gabriela Guillena
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , [2020]
Descrizione fisica 1 online resource (387 pages)
Disciplina 547.13
Soggetto topico Physical organic chemistry
Green chemistry
ISBN 3-527-81849-9
3-527-81848-0
3-527-81847-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910830993903321
Weinheim, Germany : , : Wiley-VCH, , [2020]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Journal of the Chemical Society. Perkin transactions 2: Physical organic chemistry
Journal of the Chemical Society. Perkin transactions 2: Physical organic chemistry
Pubbl/distr/stampa London, : Chemical Society
Disciplina 541.3
547.1
547.13
ISSN 0300-9580
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Perkin transactions Transactions 2
Note periodicità Mensile
Record Nr. UNINA-990008994230403321
London, : Chemical Society
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Journal of the Chemi...