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    Molecular Beams in Physics and Chemistry From Otto Stern's Pioneering Exploits to Present-Day Feats /

    Published 2021
    Table of Contents: “…On Otto Stern, Max Born and other physicists in the 1920s (Arne Schirrmacher) -- Otto Sackur, Otto Stern, and the Beginning of the Quantum Theory of Gases (Massimiliano Badino) -- From Stern's beam experiments to modern biomolecular NMR spectroscopy (Christian Griesinger) -- Quantum or classical perception: The Imaging Theorem and the Ensemble Picture (John Briggs) -- Reduction of the atomic wave function in the Stern-­Gerlach magnetic field (Michael Devereux) -- Precision experiments for the revised SI -­ and the future of time (Joachim Ullrich) -- Precision Physics in Penning Traps Using the Continuous Stern-­Gerlach-­Effect (Klaus Blaum) -- Frankfurt Physicists (Michael Eckert) -- Our Patrimony from Otto Stern and My Memories of Otto Frisch (Dan Kleppner) -- Ultracold Chemical reactions with molecules in slow motion (Kang-Kuen Ni) -- Choreographing Quantum Spin Dynamics with Light (Monika Schleier-Smith) -- Stern's relation to Gerlach (Horst Schmidt-­Böcking) -- Manipulation and control of molecular beams (Gerard Meijer) -- Quantum effects in cold and controlled molecular dynamics (Christiane Koch) -- Otto Stern and Wave-­Particle Duality (Peter Toennies) -- Macromolecular Matter Wave Interferometry and Talbot-­Lau Deflectometry (Markus Arndt) -- Rotating rotationless: nonadiabatic alignment of the helium dimer and trimer (Maksim Kunitski) -- Grating Diffraction of Molecular Beams: Present Day Implementations of Otto Stern's Concept (Wieland Schöllkopf) -- Interaction effects in ultra cold atom systems (Dörte Blume) -- Laser cooling and magneto-­optical trapping of molecules (Mike Tarbutt) -- Microdroplet Chemistry (Dick Zare) -- TBA (Manfred Faubel) -- From Liquid Rays to Gas Rays: The Non-­Maxwellian Evaporation of Helium from Water Microjets (Gil Nathanson) -- Laser-­induced rotation and alignment of molecules in helium nanodroplets (Henrik Stapelfeldt) -- Far-from-equilibrium dynamics of molecules in helium nanodroplets (Mikhail Lemeshko).…”
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    Interface Oral Health Science 2016 Innovative Research on Biosis-Abiosis Intelligent Interface /

    Published 2017
    Table of Contents: “…Detection of Early Caries by Laser-induced Breakdown Spectroscopy -- 16. Acoustic Diagnosis Device for Dentistry -- Part V Poster Presentation Award Winners -- 17. …”
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    Organic Chemistry with a Biological Emphasis by Soderberg, Tim

    Published 2016
    Table of Contents: “…Chapter 9: Phosphate transfer reactions -- Section 1: Overview of phosphate groups -- Section 2: Phosphate transfer reactions - an overview -- Section 3: ATP, the principal phosphate group donor -- Section 4: Phosphorylation of alcohols -- Section 5: Phosphorylation of carboxylates -- Section 6: Hydrolysis of organic phosphates -- Section 7: Phosphate diesters in DNA and RNA -- Section 8: The organic chemistry of genetic engineering -- Chapter 10: Nucleophilic carbonyl addition reactions -- Section 1: Nucleophilic additions to aldehydes and ketones: an overview -- Section 2: Hemiacetals, hemiketals, and hydrates -- Section 3: Acetals and ketals -- Section 4: N-glycosidic bonds -- Section 5: Imines -- Section 5: A look ahead: addition of carbon and hydride nucleophiles to carbonyls -- Chapter 11: Nucleophilic acyl substitution reactions -- Section 1: Carboxylic acid derivatives -- Section 2: The nucleophilic acyl substitution mechanism -- Section 3: The relative reactivity of carboxylic acid derivatives -- Section 4: Acyl phosphates -- Section 5: Formation of thioesters, esters, and amides -- Section 6: Hydrolysis of thioesters, esters, and amides -- Section 7: Protein synthesis on the ribosome -- Section 8: Nucleophilic substitution at activated amides and carbamides -- Section 9: Nucleophilic acyl substitution reactions in the laboratory -- Section 10: A look ahead: acyl substitution reactions with a carbanion or hydride ion nucleophile -- Chapter 12: Reactions at the α-carbon, part I -- Section 1: Review of acidity at the α-carbon -- Section 2: Isomerization at the α-carbon -- Section 3: Aldol addition -- Section 4: α-carbon reactions in the synthesis lab - kinetic vs. thermodynamic alkylation products -- Interchapter: Predicting multistep pathways - the retrosynthesis approachChapter 13: Reactions at the α-carbon, part II -- Section 1: Decarboxylation -- Section 2: An overview of fatty acid metabolism -- Section 3: Claisen condensation -- Section 4: Conjugate addition and elimination -- Section 5: Carboxylation -- Chapter 14: Electrophilic reactions -- Section 1: Electrophilic addition to alkenes -- Section 2: Elimination by the E1 mechanism -- Section 3: Electrophilic isomerization -- Section 4: Electrophilic substitution -- Section 5: Carbocation rearrangements -- Chapter 15: Oxidation and reduction reactions -- Section 1: Oxidation and reduction of organic compounds - an overview -- Section 2: Oxidation and reduction in the context of metabolism -- Section 3: Hydrogenation of carbonyl and imine groups -- Section 4: Hydrogenation of alkenes and dehydrogenation of alkanes -- Section 5: Monitoring hydrogenation and dehydrogenation reactions by UV spectroscopy -- Section 6: Redox reactions of thiols and disulfides -- Section 7: Flavin-dependent monooxygenase reactions: hydroxylation, epoxidation, and theBaeyer-Villiger oxidation -- Section 8: Hydrogen peroxide is a harmful 'Reactive Oxygen Species' -- Chapter 16: Radical reactions -- Section 1: Overview of single-electron reactions and free radicals -- Section 2: Radical chain reactions -- Section 3: Useful polymers formed by radical chain reactions -- Section 4: Destruction of the ozone layer by a radical chain reaction -- Section 5: Oxidative damage to cells, vitamin C, and scurvy -- Section 6: Flavin as a one-electron carrier -- Chapter 17: The organic chemistry of vitamins -- Section 1: Pyridoxal phosphate (Vitamin B6) -- Section 2: Thiamine diphosphate (Vitamin B1) -- Section 3: Thiamine diphosphate, lipoamide and the pyruvate dehydrogenase reaction -- Section 4: Folate…”
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