Preface to the Second Edition xi Acknowledgments xv Abbreviations and Notations Used in This Book xvii 1 Instrumentation 1 1.1. Introduction 1 1.1.1. Overview 1 1.1.2. Sample Introduction 3 1.2. Ionization Source 4 1.2.1. Electron Ionization Source 5 1.2.2. Chemical Ionization 8 1.2.3. Other Ionization Methods 9 1.2.3.1. Electrospray Ionization 9 1.2.3.2. Desorption Ionization 12 1.3. m/z Analysis 13 1.3.1. Time-of-Flight (TOF) 13 1.3.2. Magnetic Sector 15 1.3.3. Transmission Quadrupole 17 1.3.3.1. Selected Ion Monitoring (SIM) 21 1.3.4. Quadrupole Ion Trap (QIT) 22 1.3.5. Other Types of Mass Analysis 24 1.3.5.1. Mass Spectrometry/Mass Spectrometry(MS/MS) 24 1.3.5.2. Accurate m=z Analysis 26 1.3.6. Spectral Skewing 26 1.4. Ion Detection 30 1.4.1. Electron Multiplier 32 1.4.2. Photomultiplier Detector 33 1.5. Data System 33 1.5.1. Instrument Tuning and Calibration 33 1.5.2. The Mass Spectrum 37 1.5.2.1. Production of the Mass Spectrum 37 1.5.2.2. Terminology: Ions vs. Peaks 41 1.5.3. Library Searches 41 1.5.4. Using the Data System to Analyze GC/MS Data 45 1.6. Criteria for Good-Quality Spectra 50 Additional Problems 51 Mass Spectrometric Resources on the Internet 52 References and Suggested Reading 53 2 Elemental Composition from Peak Intensities 56 2.1. Natural Isotopic Abundances 56 2.1.1. Atomic and Molecular Mass 59 2.1.2. Calculated Exact Masses and Mass Defects 60 2.2. Determining Elemental Composition from Isotope Peak Intensities 64 2.2.1. One or More Atoms of a Single Element 64 2.2.1.1. Chlorine and Bromine 64 2.2.1.2. Ion Designation and Nomenclature 70 2.2.1.3. Probability Considerations with Multiple Numbers of Atoms 71 2.2.1.4. Isotope Peak Intensity Ratios for Carbon-Containing Ions—The X + 1 Peak 74 2.2.1.5. A, A + 1, and A + 2 Elements 77 2.2.1.6. Isotope Peak Intensity Ratios for Carbon-Containing Ions—The X + 2 Peak 78 2.2.1.7. Overlapping Peak Clusters—Contributions from 13C Only 80 2.2.1.8. Silicon 82 2.2.2. Complex Isotope Clusters 83 2.2.2.1. Sulfur Dioxide 83 2.2.2.2. Diazepam 86 2.3. Obtaining Elemental Compositions from Isotope Peak Intensities 89 Examples 91 Additional Problems 96 References 98 3 Ionization, Fragmentation, and Electron Accounting 99 3.1. A Brief Review of Orbitals and Bonding 99 3.2. Even- and Odd-Electron Species 101 3.3. Site of Initial Ionization 103 3.4. Types of Fragmentation 107 3.5. The Nitrogen Rule 109 3.6. Energy Considerations in Fragmentation Processes 110 3.6.1. Fragmentation Rates 110 3.6.2. Metastable Ions 112 3.6.3. Energy Diagrams 113 3.6.4. Stevenson’s Rule 116 Additional Examples 117 Problems 119 References 120 4 Neutral Losses and Ion Series 121 4.1. Neutral Losses 121 4.1.1. Losses from the Molecular Ion 121 4.1.2. Loss of Small Molecules from Aromatic Ions 126 4.2. Low-Mass Ion Series 131 4.2.1. n-Alkane Spectra 132 4.2.2. Effect of Chain Branching on the Spectra of Aliphatic Hydrocarbons 134 4.2.3. Ion Series for Nonaromatic Compounds 136 4.2.4. Aromatic Ion Series 142 4.2.5. Use of Ion Series: Mass Chromatograms 145 Additional Problems 148 References 148 5 A Rational Approach to Mass Spectral Problem Solving 150 5.1. Guidelines for Solving Mass Spectral Problems 150 Examples 153 Problems 161 Reference 163 6 a-Cleavage and Related Fragmentations 164 6.1. Introduction 164 6.2. Benzylic Cleavage 166 6.3. Cleavage Next to Aliphatic Nitrogen 170 6.3.1. Structural Relationships: a-Cleavage in 1-Phenyl-2-aminopropanes 171 6.3.2. Cleavage Next to Electron-Deficient Nitrogen 176 6.3.3. a-Cleavage in Complex Nitrogenous Ring Systems 179 6.4. Cleavages of Aliphatic Oxygenated Compounds 180 6.4.1. a-Cleavage 180 6.4.2. Bond Cleavage Away from the Ionization Site 184 6.4.3. Cleavage at Carbonyl Groups 186 6.5. Elimination Fragmentations in Oxygen and Nitrogen Compounds 192 6.5.1. Secondary Elimination from Initial a-Cleavage Ions 192 6.5.2. Hydride Shifts 195 6.5.3. Elimination Fragmentations of Some Aromatic Compounds 196 6.5.4. Water Elimination in Aliphatic Alcohols 198 Examples 200 Additional Problems 202 References 206 7 Important Mass Spectral Rearrangements 207 7.1. Introduction 207 7.2. g-Hydrogen Rearrangement 208 7.2.1. McLafferty-Type Rearrangement 208 7.2.2. g-Hydrogen Rearrangement in Alkylbenzenes 213 7.2.3. g-Hydrogen Rearrangement Initiated by a Remote Ionization Site 217 7.3. Cyclohexanone-Type Rearrangement 223 7.4. Retro Diels–Alder Fragmentation 228 7.5. Double-Hydrogen (McLafferty + 1) Rearrangement 234 Additional Problems 236 References 237 8 Rationalizing Mass Spectral Fragmentations 238 8.1. General Guidelines 238 8.2. Loss of Small Molecules 241 8.2.1. Loss of Small Molecules from Aromatic Ions Revisited 241 8.2.2. g-Butyrolactone 243 8.3. Ephedrine 246 8.4. Ortho Effect: The Hydroxybenzoic Acids 251 Additional Problems 254 References 256 9 Structure Determination in Complex Molecules Using Mass Spectrometry 257 9.1. Introduction 257 9.2. ‘‘Designer Drugs’’ Related to MDA 258 9.3. Cocaine and Its Metabolites 262 9.3.1. Peak Correlations 263 9.3.2. Proposed Fragmentations 268 9.3.3. Application 271 9.4. Phencyclidine and Its Analogs 274 9.4.1. Fragmentations of Phencyclidine 274 9.4.2. Phencyclidine Analogs 282 9.5. A Practical Problem 284 References 285 10 Answers to Problems 287 Index 353 

An updated and unified approach to mass spectral interpretation, emphasizing the application of basic principles Electron ionization (EI) mass spectrometry–an analytical tool used by chemists to identify and quantify compounds in a complex mixture–remains an essential technique for measuring low-molecular weight compounds such as drugs, flavor and odor components, pesticides, and petroleum products. The interpretation of EI mass spectra also remains an important skill because attempts to identify compounds using computer databases do not always yield useful results. Understanding Mass Spectra: A Basic Approach, Second Edition presents the introductory-level student with the fundamental concepts of mass spectrometry, providing a useful foundation for solving basic problems in a laboratory setting. Completely revised, the Second Edition includes: A detailed overview of theory and instrumentationStep-by-step descriptions of interpretative strategiesMany fascinating real-world case studies and examplesAdditional skill-building problems with clearly explained answersEasy-to-follow explanations of all important mathematical derivationsConvenient lists and tables of information needed to identify unknownsAdditional suggested readings Containing problems and examples with a wide range of complexity, Understanding Mass Spectra emphasizes simple, practical treatments of topics such as fragmentation types and underlying mathematical relationships. Mastering these treatments allows for a solid grounding in basic principles and encourages advanced investigation. With this emphasis on comprehension, Understanding Mass Spectra, Second Edition provides a vital introduction to the field for upper-level undergraduates and beginning graduates, as well as a valuable resource for professional chemists working in analytical laboratories.

"...the author manages to go well beyond the obvious and expected explanations...[to provide] a set of guidelines to follow for successful spectral interpretation." (Journal of Chemical Education, May 2005) "Smith does an excellent job of taking readers through a myriad of basic concepts and tying them all together to develop useful skills for spectral interpretation." (CHOICE, February 2005) "This book would do well to serve as a basis for an upper level undergraduate or graduate course…" (Journal of Natural Products, February 2005)