Авторизация
Поиск по указателям
Rao C>N> — Ultra-Violet and Visible Spectroscopy: Chemical Applications
Обсудите книгу на научном форуме Нашли опечатку?
Название: Ultra-Violet and Visible Spectroscopy: Chemical ApplicationsАвтор: Rao C>N> Аннотация: It would be superfluous to stress the importance of electronic .spectroscopy in structural or analytic research. It has now become a matter of routine to record the ultra-violet or visible spectra of compounds for purposes of identification or structure elucidation. The spectrophotonletric methods of analysis have replaced the conventional methods in ever so rnany instances. The number of-publications in the different branches of chemistry, reporting data on or making use of electronic spectroscopy, is ever-increasing and it would be impossible to review the field completely. In this book, I have tried to introduce the basic concepts of electronic spectroscopy and to present its applications in analytical, structural and physico-chemical problems. As far as possible, the rnateripl has been selected to illustrate the basic: principles of modern theories in chemistry. While surveying the data on organic molecules, several empirical generalizations have been discussed. lVlany of the more recent developments like tIle far ultra-violet spectra of organic molecules, fluorescence spectra, charge transfer spectra, ligand field theory, optical rotatory dispersion etc., have been briefly discussed in the latter part of the book. All through the discussion, the recent notations of electronic transitions have been used, although the other commonly encountered notations have also been mentioned. I shall be most gratified if this book can be of help to chemists in using electronic spectroscopy more effectively in research or routine work.
Язык: Рубрика: Физика /Статус предметного указателя: Готов указатель с номерами страниц ed2k: ed2k stats Издание: 1st editionГод издания: 1961Количество страниц: 164Добавлена в каталог: 30.08.2009Операции: Положить на полку |
Скопировать ссылку для форума | Скопировать ID
Предметный указатель
Monoheterocyclic compounds 102 Mulliken’s theory 115 Mycomycin 65 N-Acyldihydroindoles 65 N-Acylindoles 65 N-Ethyl phenazyl radicals 109 N-heterocyclic compounds 102 N-Nitrosoamides 65 Naphthacene 48 101 102 naphthalene 48 53 87 101 105 108 141 Naphthaquinone 63 Naphthyl sulphonic acids 105 neo-Carotenoids 69 neo-Lycopenes 70 Nitrate ions 22 Nitro compounds 20 138 Nitro compounds, aliphatic 21 Nitro compounds, olefins 33 Nitrobenzene 43 44 Nitrobenzenes 47 Nitromethane 23 Nitroparaffins 21 Nitrophenylazide 78 Nitroso compounds 21 Nitrosobutane 11 Nitrosonium ion 134 Nomenclature of benzene bands 39 Nucleic acids 56 Nucleoproteins 57 Nucleosides 58 o-Dihydroxy benzophenone 103 Octa-3,7-dien-5-yn-2-ol 25 Octant rule 139 Olefin complexes 121 Olefins 10 16 92—94 Olefins in sulphuric acid 134 Olefins of steroid family 94 Olefins of triterpenoid family 94 Olefins, cyclic 16 94 Olefins, determination 94 Olefins, small ring 94 Optical density 3 119 Optical dichroism 121 Optical rotatory dispersion 137 Optical system 5 Optical transition, perturbation 113 Orbitals, 5 d 125 Orbitals, molecular 115 120 127 Orbitals, molecular orbital model 125 Organic compounds, fluorescence 100 Orgel diagram 129 Orientation principle 120 Osazones 75 Oscillator strength 4 Ovalbumin 149 Overlap integral 118 120 Overlap of molecular orbitals 120 Overlap principle 120 Overlap, principle of maximum overlap 321 Oxalyl chloride, complexes with aromatics 117 Oxazolone structure 65 Oximes 30 Oxyhaemoglobin 136 p-Benzoquinone 32 134 p-Chloroaniline 45 p-Chlorophenol 45 P-Dinitrobenzene 44 p-Hydroxyacetophenone 45 p-Hydroxybenzaldehyde 45 p-Hydroxybenzoic acid 45 p-Nitroaniline 44 121 p-Nitroaniline derivatives 85 p-Nitrophenol 44 45 p-Xylene 95 Palmitates 101 Para-polyphenyls 35 Paracyclophanes 90 Paraffins 10 15 Paramagnetic atoms 99 Patulin 68 Penamaldates 64 Penicillins 64 Penicilloates 64 Penicilloates, N-acetylated 64 Pentacene 48 101 Pentazoles 53 Perylene 101 107 pH effect 148 pH, dependence of fluorescence on pH 105 Phellandrenes 66 Phenanthrene 48 87 95 101 107 141 Phenazine 53 102 Phenol 41 45 105 Phenol, blue 141 Phenols 47 144 Phenylbenzoates 47 Phosphonitrilic chlorides 50 phosphors 104 Photo-excitation 112 Photochemical isomerization 106 Photoreduction 100 Phthalazine 53 Picrates 111 Pigments 134 Pigments, visual 135 Piperazine 52 Piperidine 52 Piperylene 27 Plasma albumin, bovine 149 Platinum cyanide radical 104 Pleochromism 107 Polarization of fluorescent light 107 Polarization, forces of solvents 140 Polarization, red shift 140 Polyacetylenes 36 Polyalkyl azulenes 49 Polyene acids 33 Polyene azines 35 Polyene azomethines 35 Polyene complexes with Lewis acid 134 Polyenes 33 69 135 Polymers of dye molecules 137 Polypeptides 139 Polyphenyl derivatives 42 Polyphenyls 35 polystyrene 74 Porphyrin 102 104 135 Potassium azide 133 Potassium bromide pellets 7 Potassium dichromate 143 Potassium nitrate 143 Potential energy diagram 116 Predissociation 101 Promethium 104 Protein hydrogen bonds 148 Protein structure, co-operative changes 150 Protein-dye interactions 79 Proteins 139 148 Purification, control 61 Purine 57 Purines 105 Purity, specification 61 Purity, specification, spectrophotometry 61 Pyrazine 12 53 54 102 Pyrethrin 67 Pyrethrolone 67 Pyridazine 54 141 Pyridine 53 102 Pyridine derivatives 55 77 Pyridine, substituted 55 Pyridine-N-oxide 56 Pyridoxine 56 Pyrimidine 53 54 56 Pyrimidine, derivatives 56 Pyrimidines 105 Pyrimidones 56 Pyrrol 102 Pyrrole 52 Pyrrolidine 52 Quadratic Stark effect 141 Quantum efficiency 112 Quenching 99 106 Quenching, concentration 99 Quenching, internal 99 Quinhydrone 111 121 Quinine bisulphate 100 Quinoline 53 Quinoline ions 102 Quinolines, substituted 56 Quinolium ions 102 Quinoxaline 53 Radiation, fluorescent 2 Radicals, free 134 Rare earth ions 104 Rare earths 99 Rate constants 142 Ratio method 74 Reaction rates 78 Red-shift 12 139 Regions, far ultra-violet 1 92 Regions, near ultra-violet 1 Regions, vacuum ultra-violet 1 Regions, visible 1 Repetitive scanning attachments 78 Resonance 18 Resonance effects 40 44 Resonance parameters 44 Rhodamine 60 100 Rhoduline violet 103 Rhoduline-orange 99 Ribonuclease 148 149 Ring compounds, five-membered 28 Ring size, effect 29 Rings, three-membered 90 Rosamine 103 Rotational freedom 120 Rotatory dispersion curves, Cotton effect 138 Rotatory dispersion curves, plain 138 Rubidium halides 112 Rubies 107 Rydberg series 11 Salicylic acid 143 Self complexes 121 Semicarbazones 30 Semperivinine 65 Serum albumin, bovine 149 Silica, colloidal 100 Silicates 104 Siloxene group 104 Silver halides 133 Silver ion, complexes with ethylene 121 Single bond 82 Single bond, effect of twisting 82 Sodium 99 Sodium benzene sulphonate 104 Sodium bromide 104 Sodium chloride 104 Sodium formaldehyde-sulphoxylate 104 Sodium nitrate 22 Solute dipole-induced solvent dipole interactions 140 Solute dipole-solvent dipole interactions 140 Solvation energies 116 Solvent effects 12 13 22 139 142 Solvent effects on fluorescence 103 Solvent polarity 141 Solvent-solute interaction 108 Solvents, choice 7 Solvents, hydroxylic 141 142 Sorbaldehyde 25 Specific rotation 137 Spectra of charge transfer complexes 116 Spectra of gases 7 Spectra of solids 7 Spectra, absorption 1 Spectra, electronic 1 Spectra, emission 1 Spectra, luminescent 121 Spectrophotometer accessories 8 Spectrophotometer calibration 143 Spectrophotometers, method 119 Spectrophotometers, photoelectric 5 Spectrophotometers, slit width 6 Spectrophotometry in analysis 73 Spectrophotometry, differential 148 Spectrophotometry, preferential 58 Spectropolarimeters 137 Spectroscopic moments 43 Spectroscopy, applications 61 Spectrotitrimeter 78 Spin-orbital interaction, effect of increase 104 Standard free energy 118 Standards 6 Stearates 101 Stereoisomerism 105 Stereoisomerization 106 Steric effects 82 109 114 Steric effects, Type 1 85 Steric effects, Type 2 87 Steric effects, Type 3 87 Sterols, ergosterol content 73 Stilbenes 106 strain 90 Structure S-cis form 88 Structure S-trans form 88 Structure, identification and assignment 62 Structure, skew 87 Strychnine 65 Styrene anion 134 Substituent groups, electron-attracting 44 Substituent groups, electron-contributing 44 Substituent groups, meta-directing 44 Substituent groups, ortho-para directing 44 Substituents, effects 35 43 48 Substituents, ortho 89 Sydnones 58 Sym-di-(9-phenanthry-ethylene) 106 sym-Tetrazine 55 sym-triazine 53 Tautomerism 49 55 56 70 106 Tautomerism, azo-hydrazo 73 Tautomerism, keto-enol 70 Tautomerism, thione-thiol 72 Temperature effects 142 Terramycin 65 Testosterone-enolacetate 27 Tetrahydrofuran 52 Tetrahydropyran 52 Tetrahydropyrethrolone 29 67 Tetramethylbiphenyl 83 Tetramethylthiuram disulphide 108 Tetraphenyl cumulenes 37 Tetraphenylethylene 88 Tetraphenylstiboniumdichloride 42 Tetrazole 52 Tetrazoles, substituted 59 Thallous ion 104 Theophylline 58 Thermochromism 143 Thermochromism, negative 109 Thermodynamic criteria 120
Реклама
|
|
О проекте