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Centrifugation : essential data / David Rickwood, T. Ford, J. Steensgaard
| Centrifugation : essential data / David Rickwood, T. Ford, J. Steensgaard |
| Autore | Rickwood, David |
| Pubbl/distr/stampa | Chichester, : Wiley, 1994 |
| Descrizione fisica | xi, 114 p. ; 24 cm. |
| Disciplina | 542.8(Tecniche, procedure, attrezzature, materiali della chimica inorganica e organica) |
| ISBN | 04-7194-271-5 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-SUN0018815 |
Rickwood, David
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| Chichester, : Wiley, 1994 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
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Centrifugation : essential data / David Rickwood, T. Ford, J. Steensgaard
| Centrifugation : essential data / David Rickwood, T. Ford, J. Steensgaard |
| Autore | Rickwood, David |
| Pubbl/distr/stampa | Chichester, : Wiley, 1994 |
| Descrizione fisica | xi, 114 p. ; 24 cm |
| Disciplina | 542.8(Tecniche, procedure, attrezzature, materiali della chimica inorganica e organica) |
| ISBN | 04-7194-271-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-VAN0018815 |
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Rickwood, David
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| Chichester, : Wiley, 1994 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
| ||
Centrifugation : Essential Data / David Rickwood, T. Ford, J. Steensgaard
| Centrifugation : Essential Data / David Rickwood, T. Ford, J. Steensgaard |
| Autore | Rickwood, David |
| Pubbl/distr/stampa | Chichester, : Wiley, 1994 |
| Descrizione fisica | XI, 114 p. ; 24 cm |
| Disciplina | 542.8(Tecniche, procedure, attrezzature, materiali della chimica inorganica e organica) |
| ISBN | 04-7194-271-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNICAMPANIA-VAN00018815 |
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Rickwood, David
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| Chichester, : Wiley, 1994 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Vanvitelli | ||
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Chemoinformatics approaches to virtual screening / / edited by Alexandre Varnek, Alex Tropsha
| Chemoinformatics approaches to virtual screening / / edited by Alexandre Varnek, Alex Tropsha |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Cambridge, : RSC Pub., 2008 |
| Descrizione fisica | 1 online resource (xvi, 338 pages) : illustrations (some color) |
| Disciplina | 542.8 |
| Altri autori (Persone) |
VarnekAlexandre
TropshaAlex |
| Soggetto topico |
Cheminformatics
Chemistry - Data processing |
| ISBN |
1-61583-352-8
1-84755-887-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Preface-- 1 -- Fragment Descriptors in SAR/QSAR/QSPR studies, molecular similarity analysis and in virtual screening-- Introduction-- Historical survey-- Main characteristics of Fragment Descriptors-- Types of Fragments-- Simple Fixed Types-- WLN and SMILES Fragments-- Atom-Centered Fragments-- Bond-Centered Fragments-- Maximum Common Substructures-- Atom Pairs and Topological Multiplets-- Substituents and Molecular Frameworks-- Basic Subgraphs-- Mined Subgraphs-- Random Subgraphs-- Library Subgraphs-- Fragments describing supramolecular systems and chemical reactions-- Storage of fragments' information-- Fragment's Connectivity-- Generic Graphs-- Labeling Atoms-- Application in Virtual Screening and In Silico Design-- Filtering-- Similarity Search-- SAR Classification (Probabilistic) Models-- QSAR/QSPR Regression Models-- In Silico Design-- Limitations of Fragment Descriptors-- Conclusion-- 2 -- Topological Pharmacophores-- Introduction-- 3D pharmacophore models and descriptors-- Topological pharmacophores-- Topological pharmacophores from 2D-aligments-- Topological pharmacophores from 2D pharmacophore fingerprints-- Topological index-based 'pharmacophores'?-- Topological pharmacophores from 2D-aligments-- Topological pharmacophores from pharmacophore fingerprints-- Topological pharmacophore pair fingerprints-- Topological pharmacophore triplets-- Similarity searching with pharmacophore fingerprints -- Technical Issues-- Similarity searching with pharmacophore fingerprints -- Some Examples-- Machine-learning of Topological Pharmacophores from Fingerprints-- Topological index-based 'pharmacophores'?-- Conclusions-- 3 -- Pharmacophore-based Virtual Screening in Drug Discovery-- Introduction-- Virtual Screening Methods-- Chemical Feature-based Pharmacophores-- The Term "3D Pharmacophore"-- Feature Definitions and Pharmacophore Representation-- Hydrogen bonding interactions-- Lipophilic areas-- Aromatic interactions-- Charge-transfer interactions-- Customization and definition of new features-- Current super-positioning techniques for aligning 3D pharmacophores and molecules-- Generation and Use of Pharmacophore Models-- Ligand-based Pharmacophore Modeling-- Structure-based Pharmacophore Modeling-- Inclusion of Shape Information-- Qualitative vs. Quantitative Pharmacophore Models-- Validation of Models for Virtual Screening-- Application of Pharmacophore Models in Virtual Screening-- Pharmacophore Models as Part of a Multi-Step Screening Approach-- Antitarget and ADME(T) Screening Using Pharmacophores-- Pharmacophore Models for Activity Profiling and Parallel Virtual Screening-- Pharmacophore Method Extensions and Comparisons to Other Virtual Screening Methods-- Topological Fingerprints-- Shape-based Virtual Screening-- Docking Methods-- Pharmacophore Constraints Used in Docking-- Further Reading-- Summary and Conclusion-- 4 -- Molecular Similarity Analysis in Virtual Screening-- Ligand-Based Virtual Screening-- Foundations of Molecular Similarity Analysis-- Molecular Similarity and Chemical Spaces-- Similarity Measures-- Activity Landscapes-- Analyzing the Nature of Structure-Activity Relationships-- Relationships between different SARs-- SARs and target-ligand interactions-- Qualitative SAR characterization-- Quantitative SAR characterization-- Implications for molecular similarity analysis and virtual screening-- Strengths and Limitations of Similarity Methods-- Conclusion and Future Perspectives-- 5 -- Molecular Field Topology Analysis in drug design and virtual screening-- Introduction: local molecular parameters in QSAR, drug design and virtual screening-- Supergraph-based QSAR models-- Rationale and history-- Molecular Field Topology Analysis (MFTA)-- General principles-- Local molecular descriptors: facets of ligand-biotarget interaction-- Construction of molecular supergraph-- Formation of descriptor matrix-- Statistical analysis-- Applicability control-- From MFTA model to drug design and virtual screening-- MFTA models in biotarget and drug action analysis-- MFTA models in virtual screening-- MFTA-based virtual screening of compound databases-- MFTA-based virtual screening of generated structure libraries-- Conclusion-- 6 -- Probabilistic approaches in activity prediction-- Introduction-- Biological Activity-- Dose-Effect Relationships-- Experimental Data-- Probabilistic Ligand-Based Virtual Screening Methods-- Preparation of Training Sets-- Creation of Evaluation Sets-- Mathematical Approaches-- Evaluation of Prediction Accuracy-- Single-Targeted vs. Multi-Targeted Virtual Screening-- PASS Approach-- Biological Activities Predicted by PASS-- Chemical Structure Description in PASS-- SAR Base-- Algorithm of Activity Spectrum Estimation-- Interpretation of Prediction Results-- Selection of the Most Prospective Compounds-- Conclusions-- 7 -- Fragment-based de novo design of druglike molecules-- Introduction--From Molecules to Fragments-- From Fragments to Molecules-- Scoring the Design-- Conclusions and Outlook-- 8 -- Early ADME/T predictions: a toy or a tool?-- Introduction-- Which properties are important for early drug discovery?-- Physico-chemical profiling-- Lipophilicity-- Solubility-- Data availability and accuracy-- Models-- Why models don't work: the challenge of the Applicability Domain-- AD based on similarity in the descriptor space-- AD based on similarity in the property-based space-- How reliable are predictions of physico-chemical properties?-- Available Data for ADME/T biological properties-- Absorption-- Data-- Models-- Distribution-- Data-- Models-- The usefulness of ADME/T models is limited by available data-- Conclusions-- 9 -- Compound Library Design -- Principles and Applications-- Introduction to Compound Library Design-- Methods for Compound Library Design-- Design for Specific Biological Activities-- Similarity Guided Design of Targeted Libraries-- Diversity Based Design of General Screening Libraries-- Pharmacophore Guided Design of Focused Compound Libraries-- QSAR Based Targeted Library Design-- Protein Structure Based Methods for Compound Library Design-- Design for Developability or Drug-likeness-- Rule & Alert Based Approaches-- QSAR Based ADMET Models-- Undesirable Functionality Filters-- Design for Multiple Objectives and Targets Simultaneously-- Concluding Remarks-- 10 -- Integrated Chemo- and Bioinformatics Approaches to Virtual Screening-- Introduction-- Availability of large compound collections for virtual screening-- NIH Molecular Libraries Roadmap Initiative and the PubChem database-- Other chemical databases in public domain-- Structure based virtual screening-- Major methodologies-- Challenges and limitations of current approaches-- The implementation of cheminformatics concepts in structure based virtual screening-- Predictive QSAR models as virtual screening tools-- Critical Importance of model validation-- Applicability domains and QSAR model acceptability criteria-- Predictive QSAR modeling workflow-- Examples of application-- Structure based chemical descriptors of protein ligand interface: the EnTESS method-- Derivation of the EnTESS descriptors-- Validation of the EnTESS descriptors for binding affinity prediction-- Structure based cheminformatics approach to virtual screening: the CoLiBRI method-- The representation of three-dimensional active sites in multidimensional chemistry space-- The mapping between chemistry spaces of active sites and ligands-- Summary and Conclusions. |
| Record Nr. | UNINA-9911006771603321 |
| Cambridge, : RSC Pub., 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Exploring Chemical Concepts Through Theory and Computation
| Exploring Chemical Concepts Through Theory and Computation |
| Autore | Liu Shubin |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Newark : , : John Wiley & Sons, Incorporated, , 2024 |
| Descrizione fisica | 1 online resource (594 pages) |
| Disciplina | 542.8 |
| Soggetto topico |
Computational chemistry
Quantum chemistry |
| ISBN |
9783527843411
3527843418 9783527843435 3527843434 9783527843428 3527843426 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright -- Contents -- Preface -- Foreword -- 10 Questions About Exploring Chemical Concepts Through Theory and Computation -- Chapter 1 Chemical Concepts from Molecular Orbital Theory -- 1.1 Introduction -- 1.2 Molecular Orbital Theory -- 1.3 Canonical Molecular Orbitals -- 1.4 Frontier Molecular Orbital Theory -- 1.5 Localized Molecular Orbitals -- 1.5.1 Orthogonal Localized Molecular Orbitals -- 1.6 Regularized Nonorthogonal Localized Molecular Orbitals -- 1.7 Molecular Orbitalets -- Acknowledgment -- References -- Chapter 2 Chemical Concepts from Ab Initio Valence Bond Theory -- 2.1 Introduction -- 2.2 Ab Initio Valence Bond Theory -- 2.2.1 Valence Bond Self‐Consistent Field Method -- 2.2.2 Rumer Structures -- 2.2.3 Orbitals in VB Wave Function -- 2.2.4 VB Methods Involving Dynamic Correlation -- 2.3 Chemical Concepts in VB Theory -- 2.3.1 Resonance Theory -- 2.3.2 Conjugation, Hyperconjugation, and Aromaticity -- 2.3.3 Electron‐Pair Bonding in Valence Bond Theory -- 2.3.4 Diabatic States in Valence Bond Theory -- 2.4 A Brief Guide to Perform VB Calculations -- 2.4.1 Preparing XMVB Input Files -- 2.4.2 Reading XMVB Output Files -- 2.5 Concluding Remarks -- References -- Chapter 3 Chemical Concepts from Conceptual Density Functional Theory -- 3.1 Introduction -- 3.2 The Fundamentals: Density Functional Theory (DFT) and Kohn-Sham DFT -- 3.3 The First Derivatives: The Electronic Chemical Potential and the Electron Density -- 3.4 The Second Derivatives: Chemical Hardness, Fukui Function, Linear Response Function, and Related Quantities -- 3.4.1 Chemical Hardness and Softness -- 3.4.2 The Fukui Function and the Dual Descriptor -- 3.4.3 Local Softness and Hardness -- 3.4.4 The Linear Response Function, Softness and Hardness Kernels -- 3.5 Perturbational Perspective of Chemical Reactivity -- 3.6 Conclusions -- Acknowledgment.
References -- Chapter 4 Chemical Concepts from Density‐Based Approaches in Density Functional Theory -- 4.1 Introduction -- 4.2 Four Density‐Based Frameworks -- 4.2.1 Orbital‐Free DFT (OF‐DFT) -- 4.2.2 Conceptual DFT (CDFT) -- 4.2.3 Density‐Associated Quantities (DAQs) -- 4.2.4 Information‐Theoretic Approach (ITA) -- 4.3 Applications of Density‐Based Approaches -- 4.3.1 Molecular Isomeric and Conformational Stability -- 4.3.2 Bonding and Noncovalent Interactions -- 4.3.3 Cooperation and Frustration -- 4.3.4 Homochirality and Principle of Chirality Hierarchy -- 4.3.5 Electrophilicity and Nucleophilicity -- 4.3.6 Regioselectivity and Stereoselectivity -- 4.3.7 Brønsted-Lowry Acidity and Basicity -- 4.3.8 Aromaticity and Antiaromaticity -- 4.3.9 Molecular Properties (Frontier Orbitals, HOMO/LUMO Gap, Oxidation States, Polarizability) -- 4.4 Concluding Remarks -- Acknowledgments -- References -- Chapter 5 Chemical Bonding -- 5.1 Introduction -- 5.2 The Physical Mechanism of the Chemical Bond -- 5.3 Bonding Models -- 5.4 Bond Length and Bond Strength -- 5.5 Dative and Electron‐Sharing Bonds -- 5.6 Polar Bonds -- 5.7 Atomic Partial Charges and Atomic Electronegativity -- 5.8 Chemical Bonding in Main‐Group Compounds: N2, CO, BF, LiF -- 5.9 Chemical Bonding of the Heavier Main‐Group Atoms -- 5.10 Chemical Bonding in Transition Metal Complexes: M(CO)n (M & -- equals -- Ni, Fe, Cr, Ti, Ca -- n & -- equals -- 4 - 8) -- 5.11 Summary -- Acknowledgments -- References -- Chapter 6 Partial Charges -- 6.1 Concept of Partial Charge -- 6.1.1 What is Partial Charge? -- 6.1.2 Theoretical Significances and Practical Applications of Partial Charge -- 6.1.3 Limitations of Partial Charge -- 6.1.4 What Is a Good Method of Calculating Partial Charges? -- 6.1.5 Classification of Partial Charge Calculation Methods -- 6.2 Methods of Calculating Partial Charges. 6.2.1 Partial Charges Based on Wavefunction -- 6.2.1.1 Mulliken Method -- 6.2.1.2 MMPA Methods -- 6.2.1.3 Löwdin Method -- 6.2.1.4 NPA Method -- 6.2.2 Partial Charges Based on Real Space Partition of Electron Density -- 6.2.2.1 AIM Method -- 6.2.2.2 Voronoi and VDD Methods -- 6.2.2.3 Hirshfeld Method -- 6.2.2.4 Hirshfeld‐I Method -- 6.2.3 Partial Charges Based on Fitting Electrostatic Potential -- 6.2.3.1 Common ESP Fitting Methods -- 6.2.3.2 RESP and Relevant Methods -- 6.2.4 Partial Charges Based on Equalization of Electronegativity -- 6.2.5 Partial Charges Based on Other Ideas -- 6.3 Partial Charges of Typical Molecules -- 6.4 Computer Codes for Evaluating Partial Charges -- 6.5 Concluding Remarks -- References -- Chapter 7 Atoms in Molecules -- 7.1 Introduction -- 7.2 The Quantum Theory of Atoms in Molecules (QTAIM) -- 7.3 QTAIM Atoms as Open Quantum Systems -- 7.3.1 Sector Density Operators of Quantum Atoms in Molecules -- 7.3.2 RDMs of Atoms in Molecules -- 7.4 Interacting Quantum Atoms (IQA) -- References -- Chapter 8 Effective Oxidation States Analysis -- 8.1 The Concept of Oxidation State -- 8.2 Oxidation State is Not Related to the Partial Charge -- 8.3 The Molecular Orbital Picture of the Ionic Approximation -- 8.4 Spin‐Resolved Effective Fragment Orbitals and Effective Oxidation States (EOS) Analysis -- 8.5 EOS Analysis from Different AIM Schemes -- 8.6 Summary -- References -- Chapter 9 Aromaticity and Antiaromaticity -- 9.1 Definition of Aromaticity -- 9.2 Physical Foundation -- 9.3 Measures of Aromaticity -- 9.3.1 Geometric Descriptors of Aromaticity -- 9.3.2 Energetic Descriptors of Aromaticity -- 9.3.3 Electronic Descriptors of Aromaticity -- 9.3.4 Magnetic Descriptors of Aromaticity -- 9.4 Rules of Aromaticity -- 9.4.1 Rules for Two‐Dimensional Aromaticity -- 9.4.2 Rules for Three‐Dimensional Aromaticity. 9.5 Metallabenzenes and Related Compounds as an Example -- References -- Chapter 10 Acidity and Basicity -- 10.1 Introduction -- 10.2 Definitions and Theories -- 10.2.1 Arrhenius Theory -- 10.2.2 Brønsted-Lowry Theory -- 10.2.3 Lewis Theory -- 10.2.4 Usanovich Definition -- 10.2.5 Lux-Flood Definition -- 10.2.6 Solvent System Definition -- 10.3 CDFT‐Based Reactivity Descriptors -- 10.4 CDFT‐Based Electronic Structure Principles -- 10.4.1 Equalization Principles -- 10.4.2 Hard-Soft Acid-Base (HSAB) Principle -- 10.4.3 Maximum Hardness (MHP), Minimum Polarizability (MPP), and Minimum Electrophilicity (MEP) Principles -- 10.5 Systemics of Lewis Acid-Base Reactions: Drago-Wayland Equation -- 10.6 Strengths of Acid and Bases -- 10.6.1 Ionic Product -- 10.6.2 pH Scale -- 10.6.3 Ionization Constants -- 10.6.4 Proton Affinity -- 10.6.5 Electronegativity -- 10.6.6 Hardness -- 10.6.7 Electrophilicity -- 10.7 Effect of External Perturbation -- 10.7.1 Steric Effects -- 10.7.2 Solvent Effects -- 10.7.3 Periodicity -- 10.7.4 Inductive Effect -- 10.7.5 Resonance Effect -- 10.8 CDFT and Acidity -- 10.9 CDFT and ITA -- 10.10 Are Strong Brønsted Acids Necessarily Strong Lewis Acids? -- 10.11 Summary -- Acknowledgment -- Conflict of Interest -- References -- Chapter 11 Sigma Hole Supported Interactions: Qualitative Features, Various Incarnations, and Disputations -- 11.1 Introduction -- 11.1.1 What's in a Name - The Sigma Hole Terminology and Concept -- 11.1.2 Donor-Acceptor Interaction Continuum -- 11.2 Many Incarnations and Roles of a Single Phenomenon -- 11.2.1 Hydrogen Bonding -- 11.2.2 Halogen Bonding and Sigma Holes on Group 17 Atoms -- 11.2.2.1 Common Origins -- 11.2.2.2 Cases of Halogen Bonding -- 11.2.2.3 The Sigma Hole and the Whole Story -- 11.2.3 Chalcogens -- 11.2.4 Pnictogens -- 11.2.5 Tetrels -- 11.2.6 Triels. 11.3 Related Interactions Elsewhere in the Main Group -- 11.3.1 Group 2 -- 11.3.2 Group 1 -- 11.3.3 Group 18 -- 11.4 Contested Interpretations -- 11.5 Conclusions -- Acknowledgment -- References -- Chapter 12 On the Generalization of Marcus Theory for Two‐State Photophysical Processes -- 12.1 Introduction -- 12.2 The Golden Rule Rate Expression -- 12.2.1 The Marcus Theory: The Classical Treatment -- 12.2.2 The Marcus-Levich-Jortner Expression: A Quantum Expression for High‐Frequency Modes -- 12.2.3 The Föster Theory: Separating Donor and Acceptor Parts in FCWD -- 12.3 Application -- 12.3.1 Electron Transfer -- 12.3.2 SET: Using Spectra for FCWD -- 12.3.3 TET and Other Energy Transfer Process with Spin Exchange -- 12.4 Conclusion -- Acknowledgments -- References -- Chapter 13 Computational Modeling of CO2 Reduction and Conversion via Heterogeneous and Homogeneous Catalysis -- 13.1 Introduction -- 13.2 Computational Methods -- 13.3 Activation and Reduction of CO2 -- 13.3.1 Computational Catalyst Design -- 13.3.1.1 Doping of Metal and Nonmetal Atoms -- 13.3.1.2 Structural Modification -- 13.3.1.3 Application of an External Electric Field -- 13.3.2 Electrocatalytic Reduction of CO2 -- 13.3.3 Hydrogenation Reduction of CO2 -- 13.4 Catalytic Coupling of CO2 with CH4 -- 13.5 Homogeneous Catalytic Conversion of CO2 -- 13.5.1 Catalytic CO2 Fixation into Cyclic Carbonates -- 13.5.2 CO2 Hydrogenation Catalyzed by Metal PNP‐Pincer Complexes -- 13.6 Conclusion and Outlook -- Acknowledgments -- References -- Chapter 14 Excited States in Conceptual DFT -- 14.1 Introduction -- 14.2 Exploring Ground State Properties Thanks to Excited States -- 14.2.1 Context and Justification -- 14.2.2 Chemical Hardness Revisited -- 14.2.3 State‐Specific Dual Descriptors -- 14.2.4 Polarization Interaction -- 14.3 Exploring the Reactivity of Excited States with Excited States. 14.3.1 Local Chemical Potential. |
| Record Nr. | UNINA-9911019420803321 |
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Liu Shubin
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| Newark : , : John Wiley & Sons, Incorporated, , 2024 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Lasers in chemistry / Maximilian Lackner (Ed.)
| Lasers in chemistry / Maximilian Lackner (Ed.) |
| Pubbl/distr/stampa | Wheinheim : Wiley-VCH, copyr. 2008- |
| Descrizione fisica | v. : ill. ; 25 cm |
| Disciplina | 542.8 |
| Soggetto topico | Laser -- Impiego in chimica |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-990003174130203316 |
| Wheinheim : Wiley-VCH, copyr. 2008- | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Perspectives in drug discovery and design
| Perspectives in drug discovery and design |
| Pubbl/distr/stampa | Dordrecht : Kluwer Academic Publ |
| Descrizione fisica | v. : ill. |
| Disciplina | 542.8 |
| ISSN | 0928-2866 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | dut |
| Note periodicità | Annuale |
| Record Nr. | UNISA-990001017830203316 |
| Dordrecht : Kluwer Academic Publ | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Reviews in computational chemistry
| Reviews in computational chemistry |
| Pubbl/distr/stampa | Weinheim : VCH-Wiley |
| Descrizione fisica | v. : ill. |
| Disciplina | 542.8 |
| Soggetto topico | Chimica -- Periodici |
| ISSN | 1069-3599 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Note periodicità | Annuale |
| Record Nr. | UNISA-990001055410203316 |
| Weinheim : VCH-Wiley | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Vol.1: Probing matter / Maximilian Lackner (Ed.)
| Vol.1: Probing matter / Maximilian Lackner (Ed.) |
| Pubbl/distr/stampa | Wheinheim : Wiley-VCH, copyr. 2008 |
| Descrizione fisica | XLIV, 695 p. : ill. ; 25 cm |
| Disciplina | 542.8 |
| Soggetto topico | Laser - Impiego in chimica |
| ISBN | 978-3-527-31997-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-990003174180203316 |
| Wheinheim : Wiley-VCH, copyr. 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Vol.2: Influencing matter / Maximilian Lackner (Ed.)
| Vol.2: Influencing matter / Maximilian Lackner (Ed.) |
| Pubbl/distr/stampa | Wheinheim : Wiley-VCH, copyr. 2008 |
| Descrizione fisica | XLIV, 1466 p. : ill. ; 25 cm |
| Disciplina | 542.8 |
| Soggetto topico | Laser - Impiego in chimica |
| ISBN | 978-3-527-31997-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-990003174200203316 |
| Wheinheim : Wiley-VCH, copyr. 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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