Books by Ian Fleming

Portrait of Ian Fleming

Ian Fleming, the creator of the legendary secret agent James Bond, brought a new edge of sophistication and danger to twentieth‑century spy fiction. Drawing on his own experiences in naval intelligence, Fleming combined authentic detail with razor‑sharp style, crafting stories that captured post‑war intrigue and glamour in equal measure.

From the high‑stakes casinos of Monte Carlo to shadowy Cold War battlegrounds, his novels defined the modern thriller and shaped an enduring cultural icon. Fleming's writing remains brisk, witty and steeped in atmosphere, ensuring that each adventure continues to captivate readers seeking both escapism and precision‑tooled suspense.

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82 products


  • Spectroscopic Methods in Organic Chemistry

    Springer Nature Switzerland AG Spectroscopic Methods in Organic Chemistry

    2 in stock

    Book SynopsisThis book is a well-established guide to the interpretation of the mass, ultraviolet, infrared and nuclear magnetic resonance spectra of organic compounds. It is designed for students of organic chemistry taking a course in the application of these techniques to structure determination. The text also remains useful as a source of data for organic chemists to keep on their desks throughout their career. In the seventh edition, substantial portions of the text have been revised reflecting knowledge gained during the author's teaching experience over the last seven years. The chapter on NMR has been divided into two separate chapters covering the 1D and 2D experiments. The discussion is also expanded to include accounts of the physics at a relatively simple level, following the development of the magnetization vectors as each pulse sequence is introduced. The emphasis on the uses of NMR spectroscopy in structure determination is retained. Worked examples and problem sets are included on a chapter level to allow students to practise their skills by determining the chemical structures of unknown compounds.Table of ContentsChapter 1: Mass spectra 1.1 Introduction 1.2 Ion production 1.2.1 Electron impact (EI) 1.2.2 Chemical Ionisation (CI) 1.2.3 Electrospray ionisation (ESI) 1.2.4 Fast ion bombardment (FIB or LSIMS) 1.2.5 Laser desorption (LD) and matrix-assisted laser desorption (MALDI) 1.3 Ion analysis 1.3.1 Magnetic analysers 1.3.2 Time-of–flight (TOF) analysers 1.3.3 Quadrupole analysers 1.3.4 Ion cyclotron resonance (ICR) analysers 1.3.5 Ion-trap analysers 1.4 Structural information from EI mass spectra 1.4.1 The features of an EI spectrum 1.4.2 The molecular ion 1.4.3 Isotopic abundances 1.4.4 Identifying the molecular ion 1.4.5 Fragmentation in EI spectra 1.5 Fragmentation in CI and FIB spectra 1.5.1 Fragmentation in CI spectra 1.5.2 Fragmentation in FIB (LSMIS) spectra 1.6 Some examples of mass spectrometry in action 1.6.1 San Joaquin oil 1.6.2 Oleic acid 1.6.3 The oviposition pheromone 1.6.4 Identifying antibodies 1.6.5 The ESI spectra of melittin and the human parathyroid hormone 1.6.6 ESI-FT-ICR and ESI-FT-Orbitrap spectra 1.7 Separation coupled to mass spectrometry 1.7.1 GC/MS and LC/MS 1.7.2 MS/MS 1.8 Interpreting the spectrum of an unknown 1.9 Internet 1.10 Bibliography 1.11 Problems 1.12 Tables of data Chapter 2: Ultraviolet and visible spectra 2.1 Introduction 2.2 Chromophores 2.3 The absorption laws 2.4 Measurement of the spectrum 2.5 Vibrational fine structure 2.6 Selection rules and intensity 2.7 Solvent effects 2.8 Searching for a chromophore 2.9 Definitions 2.10 Conjugated dienes 2.11 Polyenes and poly-ynes 2.12 Ketones and aldehydes; p®p* transitions 2.13 Ketones and aldehydes; n®p* transitions 2.14 a,b-Unsaturated acids, esters, nitriles and amides 2.15 Aromatic compounds 2.16 Quinones 2.17 Corroles, chlorins and porphyrins 2.18 Non-conjugated interacting chromophores 2.19 The effect of steric hindrance to coplanarity 2.20 Internet 2.21 Bibliography 2.22 Problems Chapter 3: Infrared spectra 3.1 Introduction 3.2 Preparation of samples and examination in an infrared spectrometer 3.3 Selection rules 3.4 The infrared spectrum 3.5 The use of the tables of characteristic group frequencies 3.6 Stretching frequencies of single bonds to hydrogen 3.7 Stretching frequencies of triple and cumulated double bonds 3.8 Stretching frequencies in the double-bond region 3.9 Characteristic vibrations of aromatic rings 3.10 Groups absorbing in the fingerprint region 3.11 Raman spectra 3.12 Internet 3.13 Bibliography 3.14 Problems 3.15 Correlation charts 3.16 Tables of data Chapter 4: 1D-NMR spectra 4.1 Nuclear spin and resonance 4.2 Taking a spectrum 4.3 The chemical shift 4.4 Factors affecting the chemical shift 4.4.1 The inductive effect 4.4.2 Anisotropy of chemical bonds 4.4.3 Polar effects of conjugation 4.4.4 Van der Waals forces 4.4.5 Isotope effects 4.4.6 Estimating a chemical shift 4.4.7 Hydrogen bonds 4.4.8 Solvent effects and temperature 4.5 Spin-spin coupling to 13C 4.5.1 13C-2H Coupling 4.5.2 13C-1H Coupling 4.5.3 13C-13C Coupling 4.6 1H-1H Coupling—multiplicity and coupling patterns 4.6.1 1H-1H Vicinal coupling (3JHH) 4.6.2 AB systems 4.6.3 1H-1H Geminal coupling (2JHH) 4.6.4 1H-1H Long-range coupling (4JHH and 5JHH) 4.6.5 Deviations from first-order coupling 4.7 1H-1H Coupling—the magnitude of coupling constants 4.7.1 The sign of coupling constants 4.7.2 Vicinal coupling (3JHH) 4.7.3 Geminal coupling (2JHH) 4.7.4 Long-range coupling (4JHH and 5JHH) 4.7.5 C–H coupling (1JCH, 2JCH and 3JCH) 4.8 Coupling from 1H and 13C to 19F and 31P 4.8.1 13C NMR spectra of compounds containing 19F and 31P 4.8.2 1H NMR spectra of compounds containing 19F and 31P 4.9 Relaxation and its consequences 4.9.1 Longitudinal relaxation 4.9.2 Transverse relaxation and exchange 4.10 Improving the NMR spectrum 4.10.1 The effect of changing the magnetic field 4.10.2 Solvent effects 4.10.3 Shift reagents 4.11 Spin decoupling 4.11.1 Simple spin decoupling 4.11.2 Difference decoupling 4.12 Identifying spin systems—1D-TOCSY 4.13 The nuclear Overhauser effect 4.13.1 Origins 4.13.2 NOE-Difference spectra 4.14 The rotating frame of reference 4.15 Assignment of CH3, CH2, CH and fully substituted carbons in 13C NMR 4.15.1 The Attached Proton Test (APT) 4.15.2 DEPT 4.16 Hints for structure determination using 1D-NMR 4.16.1 Carbon spectra 4.16.2 Proton spectra 4.17 Further information 4.17.1 The internet 4.17.2 Bibliography 4.18 Tables of data Chapter 5: 2D-NMR spectra 5.1 The basic pulse sequence 5.2 COSY 5.2.1 Cross peaks from scalar coupling 5.2.2 Polarisation transfer 5.2.3 The origin of cross peaks 5.2.4 Displaying COSY spectra 5.2.5 Interpreting COSY spectra 5.2.6 Axial peaks 5.2.7 Gradient pulses 5.2.8 DQF-COSY 5.2.9 Phase structure in COSY spectra 5.3 2D-TOCSY 5.4 NOESY 5.5 Cross-correlated 2D spectra identifying 1-bond connections 5.5.1 Heteronuclear Multiple Quantum Coherence (HMQC) spectra 5.5.2 Heteronuclear Single Quantum Coherence (HSQC) spectra 5.5.3 Examples of HSQC spectra 5.5.4 Non-uniform sampling (NUS) 5.5.5 Cross-peak detail—determining the sign of coupling constants 5.5.6 CLIP-HSQC 5.5.7 Deconvoluting a 1H spectrum using the HSQC spectrum 5.5.8 HSQC-TOCSY 5.5.9 HETCOR 5.6 Cross-correlated 2D spectra identifying 2- and 3-bond connections 5.6.1 The HMBC pulse sequence 5.6.2 HMBC spectra 5.7 Some specialised NMR techniques 5.7.1 ADEQUATE—identifying 13C-13C connections 5.7.2 INADEQUATE—identifying 13C-13C connections 5.7.3 HSQC-HECADE—measuring the sign and magnitude of 13C-1H coupling constants 5.8 Three- and four-dimensional NMR 5.9 Hints for structure determination using 2D-NMR 5.10 Bibliography 5.11 Table of information Chapter 6: Worked examples in structure determination 6.1 General approach 6.2 Simple worked examples using 13C NMR alone 6.3 Simple worked examples using 1H NMR alone 6.4 Simple worked examples using the combined application of MS, UV, IR and 1D-NMR spectroscopic methods 6.5 Simple worked examples using the combined application of MS, UV, IR and 1D-NMR and 2D-NMR spectroscopic methods Chapter 7: Problem sets 7.1 Chemical shift problems 7.2 1D-NMR chemical shift and coupling problems 7.3 Problems using all the spectroscopic methods Answers to problems 1-34 Index

    2 in stock

    £52.24

  • From a View to a Kill

    Travelman Publishing From a View to a Kill

    7 in stock

    Book Synopsis

    7 in stock

    £18.99

  • Chitty Chitty Bang Bang The Magical Car

    Candlewick Press,U.S. Chitty Chitty Bang Bang The Magical Car

    10 in stock

    Book Synopsis

    10 in stock

    £8.54

  • Supervision and Clinical Psychology

    Taylor & Francis Ltd Supervision and Clinical Psychology

    1 in stock

    Book SynopsisWhat are the developments influencing supervision in clinical psychology?Supervision is crucial to good professional practice and an essential part of training and continuing professional development. This second edition of Supervision and Clinical Psychology has been fully updated to include the recent developments in research, policy and the practice of supervision. With contributions from senior trainers and clinicians who draw on both relevant research and their own experience, this book is rooted in current best practice and provides a clear exposition of the main issues important to supervision. New areas of discussion include: the impact of the recent NHS policy developments in supervisor training practical aspects of supervision a consideration of future trends. Supervision and Clinical Psychology, Second Edition is essential reading for clinical psychologyTrade Review"This book, now in its second edition, offers an excellent introduction to the literature on clinical supervision, as well as invaluable practical advice for professionals. The authors review a comprehensive body of research into what works (and what doesn't) in clinical supervision, and give clear advice for clinical psychologists, psychiatrists, social workers, psychotherapists and others. I recommend it unreservedly." - Peter Kinderman, University of Liverpool, UK"The thread running throughout the book is a focus on supervision in clinical psychology and looks at many aspects of the profession. The authors consider how clinical psychology has evolved over time, in terms of Agenda for Change, and how clinical psychology jobs and training have altered. They also provide a historical overview of how clinical psychology has evolved as a profession in the context of policy change and an evolving NHS. For the past few years IAPT has developed considerably, and the authors provide the reader with a good understanding of new directions in therapy practice within the NHS for clinical psychologists and other professionals working in the service... An invaluable resource for clinicians who provide supervision across many different types of therapeutic practice." - Rob Aston, Therapy Today, February 2012'This book, now in its second edition, offers an excellent introduction to the literature on clinical supervision, as well as invaluable practical advice for professionals. The authors review a comprehensive body of research into what works (and what doesn't) in clinical supervision, and give clear advice for clinical psychologists, psychiatrists, social workers, psychotherapists and others. I recommend it unreservedly.' - Peter Kinderman, University of Liverpool, UK"The thread running throughout the book is a focus on supervision in clinical psychology and looks at many aspects of the profession. The authors consider how clinical psychology has evolved over time, in terms of Agenda for Change, and how clinical psychology jobs and training have altered. They also provide a historical overview of how clinical psychology has evolved as a profession in the context of policy change and an evolving NHS. For the past few years IAPT has developed considerably, and the authors provide the reader with a good understanding of new directions in therapy practice within the NHS for clinical psychologists and other professionals working in the service... An invaluable resource for clinicians who provide supervision across many different types of therapeutic practice." - Rob Aston, Therapy Today, February 2012Table of ContentsFleming, Steen, Introduction. Wheeler, Cushway, Supervision and Clinical Psychology: Past, Present and Future. Turpin, The Impact of Recent NHS Policy on Supervision in Clinical Psychology. Beinart, Models of Supervision and the Supervisory Relationship. Green, Generic or Model Specific Supervision? Fleming, Developments in Supervisor Training. Patel, Difference and Power in Supervision: The Case of Culture and Racism. Aitken, Dennis, Incorporating Gender Issues in Clinical Supervision. Milne, Leck, James, Watson, Proctor, Ramm, Wilkinson, Weetman. High Fidelity in Supervision Research. Steen, Formats of Supervision. Hughes, Practical Aspects of Supervision (All You Wanted to Know and Were Afraid to Ask). Fleming, Steen, Conclusions.

    1 in stock

    £109.25

  • Molekülorbitale und Reaktionen organischer

    Wiley-VCH Verlag GmbH Molekülorbitale und Reaktionen organischer

    1 in stock

    Book SynopsisDer lang erwartete Nachfolger des Lehrbuchklassikers "Grenzorbitale und Reaktionen organischer Verbindungen". Die Molekülorbitaltheorie und zahlreiche andere Themen ergänzt diese vollständig überarbeitete und aktualisierte Auflage. Mit Hilfe der Molekülorbitaltheorie kann die Verteilung von Elektronen in Molekülen beschrieben werden. Sie erlaubt somit eine Voraussage über den räumlichen Bau, die physikalischen Eigenschaften und die Reaktivität von chemischen Verbindungen. Die Molekülorbitaltheorie wird hier leicht verständlich und unter Vermeidung einer komplexen mathematischen Behandlung erklärt und mit vielen illustrativen Beispielen untermauert. Dieses Buch ist eine "Pflichtlektüre" für alle fortgeschrittenen Bachelorstudenten, Masterstudenten und Doktoranden.Trade Review"Diese vollständig überarbeitete und aktualisierte Auflage wurde um die Behandlung der Molekülorbitale und zahlreiche weitere Themen ergänzt. Dieses Buch ist eine "Pflichtlektüre" für alle fortgeschrittenen Bachelorstudenten, Masterstudenten und Doktoranden." www.amazon.de (23.03.2015)Table of ContentsVorwort XIII 1 Molekülorbitaltheorie 1 1.1 Die Atomorbitale des Wasserstoffatoms 1 1.2 Aus Wasserstoffatomen aufgebaute Moleküle 2 1.3 C—H- und C—C-Bindungen 11 1.4 Konjugation: Die Hückel-Theorie 26 1.5 Aromatizität 38 1.6 Gespannte s-Bindungen: Cyclopropane und Cyclobutane 46 1.7 Heteronukleare C—M-, C—X- und C——O-Bindungen 50 1.8 Das Tau-Bindungsmodell 61 1.9 Spektroskopische Methoden 62 2 Strukturen organischer Verbindungen 69 2.1 Der Einfluss der p-Konjugation 69 2.2 s-Konjugation: Hyperkonjugation 82 2.3 Konfiguration und Konformation von Molekülen 96 2.4 Andere nichtkovalente Wechselwirkungen 106 3 Chemische Reaktionen: Thermodynamik und Kinetik 115 3.1 Einflüsse auf die Gleichgewichtslage 115 3.2 Das Prinzip der harten und weichen Säuren und Basen (HSAB) 115 3.3 Übergangszustände 120 3.4 Störungstheoretische Behandlung der chemischen Reaktivität 122 3.5 Die Salem–Klopman-Gleichung 124 3.6 Harte und weiche Nukleophile und Elektrophile 128 3.7 Andere Faktoren, die die chemische Reaktivität beeinflussen 129 4 Ionische Reaktionen: Reaktivität 131 4.1 Elektronentransfer (ET) in ionischen Reaktionen 131 4.2 Nukleophilie 135 4.3 Ambidente Nukleophile 142 4.4 Elektrophilie 157 4.5 Ambidente Elektrophile 161 4.6 Carbene 172 5 Ionische Reaktionen: Stereochemie 179 5.1 Die Stereochemie der grundlegenden organischen Reaktionen 181 5.2 Diastereoselektivität 196 6 Thermische pericyclische Reaktionen 217 6.1 Die vier Klassen pericyclischer Reaktionen 218 6.2 Beweise für den konzertierten Verlauf der Bindungsbildungen und Bindungsbrüche 221 6.3 Symmetrieerlaubte und symmetrieverbotene Reaktionen 222 6.4 Begründungen der Woodward−Hoffmann-Regeln 251 6.5 Sekundäre Effekte 260 7 Radikalreaktionen 319 7.1 Nukleophile und elektrophile Radikale 319 7.2 Die Abstraktion von Wasserstoff- und Halogenatomen 322 7.3 Die Addition von Radikalen an p-Bindungen 324 7.4 Die Chemoselektivität von Radikalen: Synthetische Anwendungen 332 7.5 Die Stereochemie in einigen Radikalreaktionen 334 7.6 Ambidente Radikale 336 7.7 Radikalkupplungen 343 8 Photochemische Reaktionen 347 8.1 Grundsätzliches zu photochemischen Reaktionen 347 8.2 Ionische Photoreaktionen 350 8.3 Photochemische pericyclische Reaktionen und verwandte schrittweise Reaktionen 353 8.4 Photochemisch induzierte Radikalreaktionen 373 8.5 Chemilumineszenz 375 Literatur 379 Stichwortverzeichnis 383

    1 in stock

    £52.25

  • Cross Cult James Bond 007 Bd 03 Moonraker

    3 in stock

    Book Synopsis

    3 in stock

    £12.16

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  • Cross Cult James Bond 007 Bd 08 In tdlicher Mission

    2 in stock

    Book Synopsis

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  • Cross Cult James Bond 007 Bd. 09. Feuerball

    15 in stock

    Book Synopsis

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    £12.16

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    £12.16

  • Molecular Orbitals and Organic Chemical Reactions

    John Wiley & Sons Inc Molecular Orbitals and Organic Chemical Reactions

    Book SynopsisWinner of the PROSE Award for Chemistry & Physics 2010 Acknowledging the very best in professional and scholarly publishing, the annual PROSE Awards recognise publishers'' and authors'' commitment to pioneering works of research and for contributing to the conception, production, and design of landmark works in their fields. Judged by peer publishers, librarians, and medical professionals, Wiley are pleased to congratulate Professor Ian Fleming, winner of the PROSE Award in Chemistry and Physics for Molecular Orbitals and Organic Chemical Reactions. Molecular orbital theory is used by chemists to describe the arrangement of electrons in chemical structures. It is also a theory capable of giving some insight into the forces involved in the making and breaking of chemical bondsthe chemical reactions that are often the focus of an organic chemist''s interest. Organic chemists with a serious interest in understanding and explaining their work usually express their Trade Review"Fleming uses nonquantitative molecular orbital theory to explain many common phenomena in organic chemistry. As such, this is a very powerful tool for students of advanced organic chemistry. Much of what is taken simply on faith or with some hand waving in sophomore organic chemistry can be readily explained with molecular orbital theory, which is usually considered too advanced for students at that level. Though this book could be used as theprimary textbook for a course solely on molecular orbitals in organic chemistry, it will more likely be used as a reference source for an advanced organic chemistry course for upper-level undergraduates or graduate students." (CHOICE, August 2010) "The new 'Fleming' is a must for every lecturer and every student of chemistry—a fantastic book. In this new form the textbook will last for another 30 years and remain as fresh as did its predecessor!" (Angewandte Chemie International Edition March 2010)Table of ContentsPreface. 1 Molecular Orbital Theory. 1.1 The Atomic Orbitals of a Hydrogen Atom. 1.2 Molecules made from Hydrogen Atoms. 1.3 C—H and C—C Bonds. 1.4 Conjugation—Hückel Theory. 1.5 Aromaticity. 1.6 Strained σ Bonds—Cyclopropanes and Cyclobutanes. 1.7 Heteronuclear Bonds, C—M, C—X and C=O. 1.8 The Tau Bond Model. 1.9 Spectroscopic Methods. 1.10 Exercises. 2 The Structures of Organic Molecules. 2.1 The Effects of π Conjugation. 2.2 σ Conjugation—Hyperconjugation. 2.3 The Configurations and Conformations of Molecules. 2.4 Other Noncovalent Interactions. 2.5 Exercises. 3 Chemical Reactions—How Far and How Fast. 3.1 Factors Affecting the Position of an Equilibrium. 3.2 The Principle of Hard and Soft Acids and Bases (HSAB). 3.3 Transition Structures. 3.4 The Perturbation Theory of Reactivity. 3.5 The Salem-Klopman Equation. 3.6 Hard and Soft Nucleophiles and Electrophiles. 3.7 Other Factors Affecting Chemical Reactivity. 4 Ionic Reactions—Reactivity. 4.1 Single Electron Transfer (SET) in Ionic Reactions. 4.2 Nucleophilicity. 4.3 Ambident Nucleophiles. 4.4 Electrophilicity. 4.5 Ambident Electrophiles. 4.6 Carbenes. 4.7 Exercises. 5 Ionic Reactions—Stereochemistry. 5.1 The Stereochemistry of the Fundamental Organic Reactions. 5.2 Diastereoselectivity. 5.3 Exercises. 6 Thermal Pericyclic Reactions. 6.1 The Four Classes of Pericyclic Reactions. 6.2 Evidence for the Concertedness of Bond Making and Breaking. 6.3 Symmetry-Allowed and Symmetry-Forbidden Reactions. 6.4 Explanations for the Woodward-Hoffmann Rules. 6.5 Secondary Effects. 6.6 Exercises. 7 Radical Reactions. 7.1 Nucleophilic and Electrophilic Radicals. 7.2 The Abstraction of Hydrogen and Halogen Atoms. 7.3 The Addition of Radicals to π Bonds 7.4 Synthetic Applications of the Chemoselectivity of Radicals. 7.5 Stereochemistry in some Radical Reactions. 7.6 Ambident Radicals. 7.7 Radical Coupling. 7.8 Exercises. 8 Photochemical Reactions. 8.1 Photochemical Reactions in General. 8.2 Photochemical Ionic Reactions. 8.3 Photochemical Pericyclic Reactions and Related Stepwise Reactions. 8.4 Photochemically Induced Radical Reactions. 8.5 Chemiluminescence. 8.6 Exercises. References. Index.

    £111.56

  • El libro para colorear los asombrosos trabajos

    1 in stock

    Book SynopsisUn elegante y absorbente libro para colorear que ofrece cuarenta detallados dibujos creados por Rachel Ignotofsky, la autora e ilustradora de Mujeres de ciencia.Ahora, con El libro para colorear de los asombrosos trabajos de la ciencia y la naturaleza, Ignotofsky ofrece la oportunidad de formar parte de su apasionante universo artístico, y de aprender datos fascinantes mientras coloreamos. Descubriremos y exploraremos ecosistemas, desde arrecifes y selvas tropicales hasta estanques y jardines, el funcionamiento interno de una sola célula e incluso una colección de herramientas de laboratorio. Perfecta para los amantes de la naturaleza de todas las edades, esta es una encantadora guía educativa sobre el mundo en el que vivimos.

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  • Griker & Asociados, S. L. Coaching

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  • You Only Live Twice

    HarperCollins You Only Live Twice

    10 in stock

    Book SynopsisBOND TAKES ON A DEATH-DEFYING NEW MISSION TO SECURE KEY JAPANESE INTELLIGENCEJames Bond is shattered by the murder of his wife at the hands of Ernst Stavro Blofeld, and only the prospect of a particularly challenging mission can draw him out of his deep depression.Determined to restore 007 to his former effectiveness, M sends Bond to Japan, where a criminal mastermind is using a poisonous garden inside a rocky island fortress to lure people to their deaths. Bond will have to infiltrate and destroy this mysterious Castle of Death in exchange for top secret Japanese intelligence.When the mastermind behind the deadly plot proves to be an old and terrifying enemy, 007 will have to use all of his skills in a fight to the death.

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