Stereoelectronic Effects illustrates the utility of stereoelectronic concepts using structure and reactivity of organic molecules _ An advanced textbook that provides an up-to-date overview of the field, starting from the fundamental principles _ Presents a large selection of modern examples of stereoelectronic effects in organic reactivity _ Shows practical applications of stereoelectronic effects in asymmetric catalysis, photochemical processes, bioorganic chemistry and biochemistry, inorganic and organometallic reactivity, supramolecular chemistry and materials science
Stereoelectronic Effects illustrates the utility of stereoelectronic concepts using structure and reactivity of organic molecules _ An advanced textbook that provides an up-to-date overview of the field, starting from the fundamental principles _ Presents a large selection of modern examples of stereoelectronic effects in organic reactivity _ Shows practical applications of stereoelectronic effects in asymmetric catalysis, photochemical processes, bioorganic chemistry and biochemistry, inorganic and organometallic reactivity, supramolecular chemistry and materials science
Professor Igor V. Alabugin, Department of Chemistry and Biochemistry, Florida State University, USA Over the last 12 years, Professor Alabugin has published a body of work dedicated to stereoelectronic effects and applied these concepts in practice to the development of new organic reactions. The wide appeal of these concepts is reflected in a large number citations for his papers on the topic (the top three papers have well over 600 citations). His expertise is in broadly defined computational and experimental organic chemistry and its applications to medicinal chemistry and materials science.
Inhaltsangabe
Acknowledgement ix
Supplementory Material x
1 Introduction 1
1.1 Stereoelectronic effects - orbital interactions in control of structure and reactivity 1
1.2 Orbital interactions in theoretical chemistry 3
1.3 The birth of stereoelectronic concepts in organic chemistry 4
References 6
2 Direct Effects of Orbital Overlap on Reactivity 8
2.1 Bond formation without bond breaking: types of overlap in two?-orbital interactions 9
2.1.1 Factors controlling sigma?-bond overlap 12
2.2 Bond formation coupled with bond breaking 25
2.2.1 Three?-orbital interactions: stereoelectronic reasons for the preferred trajectories of intermolecular attack at a chemical bond 25
2.3 Stereoelectronics of supramolecular interactions 29
2.3.1 FMO interactions in intermolecular complexes 29
2.3.2 Expanding the palette of supramolecular interactions: from H?-bonding to Li?-, halogen, pnictogen, chalcogen and tetrel binding 30
References 36
3 Beyond Orbital Overlap: Additional Factors Important for Orbital Interactions. Classifying Delocalizing Interactions 42
3.1 Electronic count: two?]electron, one?]electron and three?]electron bonds 43
3.2 Isovalent vs. sacrificial conjugation 48
3.3 Neutral, negative, and positive hyperconjugation 49
References 52
4 Computational and Theoretical Approaches for Studies of Stereoelectronic Effects 54
4.1 Quantifying orbital interactions 54
4.2 Localized orbitals from delocalized wavefunctions 56
References 60
5 General Stereoelectronic Trends - Donors, Acceptors, and Chameleons 62
5.1 Three types of delocalization: conjugation, hyperconjugation, and sigma?-conjugation 62
5.2 Geminal and vicinal interactions 63
5.3 Stereoelectronic main rule: antiperiplanarity 64
5.3.1 Effects of bond polarity 65
5.3.2 Polarity?-induced acceptor anisotropy 68
5.4 Scales of donor and acceptor ability of orbitals: polarization, hybridization, and orbital energy effects 68
5.4.1 Donors 68
5.4.2 Acceptors 81
5.4.3 Stereoelectronic chameleons: donors masquerading as acceptors 84
5.5 Cooperativity of stereoelectronic effects and antiperiplanar lone pair hypothesis (ALPH) theory - several donors working together 91
5.6 Summary 92
References 92
6 Stereoelectronic Effects with Donor and Acceptor Separated by a Single Bond Bridge: The Broad Spectrum of Orbital Contributions to Conformational Analysis 97
6.1 sigma/sigma?-Interactions 99
6.1.1 Rotational barrier in ethane 99
6.1.2 Axial/equatorial equilibrium in methylcyclohexane 105
6.1.3 The gauche effect 110
6.2 sigma/pi?-Interactions 113
6.2.1 "Eclipsed" and "staggered" conformations of alkenes - stereoelectronic misnomers 114
1.1 Stereoelectronic effects - orbital interactions in control of structure and reactivity 1
1.2 Orbital interactions in theoretical chemistry 3
1.3 The birth of stereoelectronic concepts in organic chemistry 4
References 6
2 Direct Effects of Orbital Overlap on Reactivity 8
2.1 Bond formation without bond breaking: types of overlap in two?-orbital interactions 9
2.1.1 Factors controlling sigma?-bond overlap 12
2.2 Bond formation coupled with bond breaking 25
2.2.1 Three?-orbital interactions: stereoelectronic reasons for the preferred trajectories of intermolecular attack at a chemical bond 25
2.3 Stereoelectronics of supramolecular interactions 29
2.3.1 FMO interactions in intermolecular complexes 29
2.3.2 Expanding the palette of supramolecular interactions: from H?-bonding to Li?-, halogen, pnictogen, chalcogen and tetrel binding 30
References 36
3 Beyond Orbital Overlap: Additional Factors Important for Orbital Interactions. Classifying Delocalizing Interactions 42
3.1 Electronic count: two?]electron, one?]electron and three?]electron bonds 43
3.2 Isovalent vs. sacrificial conjugation 48
3.3 Neutral, negative, and positive hyperconjugation 49
References 52
4 Computational and Theoretical Approaches for Studies of Stereoelectronic Effects 54
4.1 Quantifying orbital interactions 54
4.2 Localized orbitals from delocalized wavefunctions 56
References 60
5 General Stereoelectronic Trends - Donors, Acceptors, and Chameleons 62
5.1 Three types of delocalization: conjugation, hyperconjugation, and sigma?-conjugation 62
5.2 Geminal and vicinal interactions 63
5.3 Stereoelectronic main rule: antiperiplanarity 64
5.3.1 Effects of bond polarity 65
5.3.2 Polarity?-induced acceptor anisotropy 68
5.4 Scales of donor and acceptor ability of orbitals: polarization, hybridization, and orbital energy effects 68
5.4.1 Donors 68
5.4.2 Acceptors 81
5.4.3 Stereoelectronic chameleons: donors masquerading as acceptors 84
5.5 Cooperativity of stereoelectronic effects and antiperiplanar lone pair hypothesis (ALPH) theory - several donors working together 91
5.6 Summary 92
References 92
6 Stereoelectronic Effects with Donor and Acceptor Separated by a Single Bond Bridge: The Broad Spectrum of Orbital Contributions to Conformational Analysis 97
6.1 sigma/sigma?-Interactions 99
6.1.1 Rotational barrier in ethane 99
6.1.2 Axial/equatorial equilibrium in methylcyclohexane 105
6.1.3 The gauche effect 110
6.2 sigma/pi?-Interactions 113
6.2.1 "Eclipsed" and "staggered" conformations of alkenes - stereoelectronic misnomers 114
6.3.3 ß?-Silicon effect and related ß?-effects 124
6.4 n/sigma?-Interactions 126
6.4.1 Anomeric effects 129
6.4.2 Reverse anomeric effect 142
6.4.3 "Anomeric effects without lone pairs": beyond the n-->sigma* interactions 143
6.5 n/pi?-Interactions 147
6.5.1 Esters and related carboxylic acid derivatives 147
6.5.2 Vinyl ethers and enamines 157
6.6 pi/pi?-Interactions 167
6.6.1 Hyperconjugation in alkynes and its relation to the "absence" o
Rezensionen
"This book is highly recommended to every chemist and particularly to every student to work through this book. The higher understanding thus obtained in many chemical fields will be beneficial throughout every phase of chemical education and work. It should furthermore be perfectly suitable as accompanying book for an advanced course on this topic." (Angewandte, 1 February 2017)
Es gelten unsere Allgemeinen Geschäftsbedingungen: www.buecher.de/agb
Impressum
www.buecher.de ist ein Shop der buecher.de GmbH & Co. KG Bürgermeister-Wegele-Str. 12, 86167 Augsburg Amtsgericht Augsburg HRA 13309
