Titel: Spectroscopic Properties of Inorganic and Organometallic Compounds: Volume 27 (Specialist Periodical Reports - Spectroscopic Properties of Inorganic and Organometallic Compounds, Volume 27)
Verlag: Royal Society of Chemistry
Erscheinungsjahr: 1993
Sprache: Englisch
ISBN-10: 0851869815
ISBN-13: 9780851869810
Einband: Hardcover
Zustand: New

�ber diesen Titel

Inhaltsangabe

Reflecting the growing volume of published work in this field, researchers will find this book an invaluable source of information on current methods and applications.

Auszug. � Genehmigter Nachdruck. Alle Rechte vorbehalten.

Spectroscopic Properties of Inorganic and Organometallic Compounds Volume 27

A Review of the Recent Literature Published up to Late 1993

By G. Davidson

The Royal Society of Chemistry

Chapter 1 Nuclear Magnetic Resonance Spectroscopy By B.E. Mann, 1, 
Chapter 2 Nuclear Quadrupole Resonance Spectroscopy By K.B. Dillon, 203, 
Chapter 3 Rotational Spectroscopy By J.H. Carpenter, 219, 
Chapter 4 Characteristic Vibrations of Compounds of Main Group Elements By G. Davidson, 246, 
Chapter 5 Vibrational Spectra of Transition Element Compounds By G. Davidson, 280, 
Chapter 6 Vibrational Spectra of Some Co-ordinated Ligands By G. Davidson, 311, 
Chapter 7 Moessbauer Spectroscopy By S.J. Clark, J.D. Donaldson, and S.M. Grimes, 357, 
Chapter 8 Gas-phase Molecular Structures Determined by Electron Diffraction By D. W.H. Rankin and H.E. Robertson, 438,

CHAPTER 1

Nuclear Magnetic Resonance Spectroscopy

BY B. E. MANN

1 Introduction

Following the criteria established in earlier volumes, only books and reviews directly relevant to this chapter are included, and the reader who requires a complete list is referred to the Specialist Periodical Reports 'Nuclear Magnetic Resonance', where a complete list of books and reviews is given. Reviews which are of direct relevance to a section of this Report are included in the beginning of that section rather than here. Papers where only 1H, 2H, 19F, and/or 31P NMR spectroscopy is used are only included when they make a non-routine contribution, but complete coverage of relevant papers is still attempted where nuclei other than these are involved. In view of the greater restrictions on space, and the ever growing number of publications, many more papers in marginal areas have been omitted. This is especially the case in the sections on solid-state NMR spectroscopy, silicon and phosphorus.

Several relevant reviews have been published, including 'Para-hydrogen-induced polarization and polarization transfer in hydrogenation and oxidative addition reactions. A mechanistic approach', 'Application of NMR techniques to organometallic compounds', 'Shift-reagent-aided 23Na NMR spectroscopy in cellular, tissue, and whole-organ systems', 'The Cinderella Nuclei', which contains 57Fe, 89Y, 103Rh, 107Ag, 109Ag, 183W, and 187Os NMR data, 'Electronic mechanisms of metal NMR chemical shifts in transition metal complexes', 'New possibilities of NMR in mechanistic studies of homogeneous and heterogeneous catalysis', which contains 13C, 17O, 51V, 59Co, and 95Mo NMR data, 'Inorganic xanthates: a structural perspective', and 'Advances in phosphorus-31 NMR'.

A number of papers have been published which are too broadly based to fit into a later section and are included here. Mass effects in the theoretical determination of nuclear spin relaxation rates for atomic hydrogen and deuterium have been examined. Nuclear shielding constants and shielding polarizabilities have been calculated for H2, N2, HF, and CO. Nuclear spin longitudinal relaxation times of deuterium gas have been interpreted in terms of relaxation of the ortho species. Ab initio calculations have been performed for 7Li in LiH, 21Ne in NeH, 23Na in NaH, and 39Ar in ArNe and Ar��NaH, as a function of internuclear separations. Nuclear singlet-triplet mixing has been analysed to understand NMR studies of homogeneous catalysis using para-hydrogen. Nuclear spin relaxation of the dihydrogen ligand in nonclassical transition metal complexes has been explained. Deuterium quadrupole coupling constants and ionic bond character in transition metal hydride complexes have been determined from 2H NMR T1 relaxation data in solution. A multiband tight binding model of the metal trihydrides, including on-site repulsion and exchange, has been examined. The nature of the high-temperature broadening of magnetic resonance lines of solvated complexes has been examined.

Trends in the 1H and 13C NMR spectra of heterobinuclear and heterotrinuclear transition-metal μ-allenyl complexes have been examined. 13C NMR spectra of ring-substituted η5-cyclopentadienyl metal complexes have been obtained using INEPT and nJ(13C1H), n = 2, 3, observed. Theoretical studies of xanthates, dixanthogen, metal xanthates, and related compounds have been used to interpret 13C NMR data. A 13C NMR study of boron, silicon, tin, phosphorus and tellurium fluorides has been reported. Empirical equations of 13C chemical shifts of the phenyl ring were deduced. NMR data have also been reported for barium, strontium, lead and zinc salts of sulfanilic acid, (13C), NiII, ZnII, CdII, and HgII complexes of poly(cinnamaldehyde-anthranilic acid), (13C), metal complexes of 4-xylosylamino-5-nitroso-6-oxopyrimidine derivatives, (13C, NiII, ZnII, CdII, and HgII complexes of pyrazine-2-carboxylic acid hydrazide and salicylidene-2-pyrazinoylhydrazine, (13C), NiII, ZnII, CdII, and HgII complexes of Z-2-benzylthio-4-hydroximinomethyl-l-p-methoxyphenyl imidazole, (13C), LiI, CuI, AgI, and CdII complexes of [C6H4(OSiMe2NBut)2]2-, (13C, 29Si), 1, (M = CaII, LaIII, ThIV, UVI, PbII; 13C), and complexes of HgCl2, CdCl2, and SbCl3 with EtNH2, Et2NH, and BuNH2, (13C).

2 Stereochemistry

This section is subdivided into eleven parts which contain NMR information about Groups 1 and 2 and transition-metal complexes presented by Groups according to the Periodic Table. Within each Group, classification is by ligand type.

Complexes of Groups 1 and 2. — Reviews have appeared entitled 'Recent results in NMR spectroscopy of organolithium compounds', 'Solution structures of lithium dialkylamides and related N-lithiated species: results from 6Li-15N double labelling experiments'. and 'Intracellular concentrations of lithium as studied by nuclear magnetic resonance spectroscopy'.

Polarization-dependent frequency shifts from rubidium-helium-3 collisions have been investigated using 3He NMR spectroscopy. 1H and 13C NMR spectroscopy has been used to study substituted pyridine-butyllithium adducts. 6Li and 13C NMR spectroscopy has been used to characterise ButLi/LiOBut mixed aggregates. 13C experimental and IGLO-calculated chemical shifts of LiCCl3 and Bun3SnR have been reported. 1J(13C13BC) =35.9 Hz and 2J(13C1H) have been determined for (C2H3)Li. (C2H3)6Li has been examined at -90 �C to give a comprehensive determination of coupling constants, including 1J(13C6Li). Sizeable J(6Li1H) values have been observed for [2-LiC6H4CH=CHLi]2 and the two inequivalent lithium resonances were assigned. 1J(13C13C) has been measured for PhLi and PhMgBr as 29.5 and 36.1 Hz respectively. The 133Cs- 1H HOESY NMR spectrum of [Ph3CCs-PMDTA]n shows agostic interactions between caesium and hydrogens. NMR data have also been reported for [MeLi.THF]4, (7Li, 13C), α,ω-Li2 polyisoprenes, (7Li), OCMe2CMe2OBCH2Li, (11B), 2, (13C) [Ph2C(C5H4N)M], {M = Li(OEt2)2, Na(THF)3, K(PMDTA); 13C, 3, (6Li), 13C [(Me3Si)3CLi(THF)2], (7Li, 13C, 29Si, including CPMAS) 4, (7Li, 13C), 5, (13C), 6 (13C), [Li(2,4,6-Pri3 C6H2)]4, (7Li, 13C), [M[phenyl bicyclo-[3.2.1]oct-3-en-2-yl)], (M = Li, K; 7Li, 13C), [(R2CO)Li{C5(SiMe2H)5}], (7Li, 13C, 29Si), [{1,4-(Me3Si)2C8H6}{Li(TMEDA)}2], (7Li, 13C), [Li2(TMEDA)2 (η5:η5-C24H14)], (13C), [K(TMEDA)2(C13H9)], (13C), [Rb(PMDTA)(C13H9)], (13C), [{(Me2N)3Si}NLiSiMe3], (13C), [(Me3Si)3SiLi(THF)3], [(Me3Si)3SiSi(SiMe3)3], (7Li, 13C, 29Si), [Cu2 {Si(SiMe3)3}2 Br-Li(THF)3], (29Si), [(PhMe2Si)3CZn (μ-Cl)2Li(THF)2], (7Li, 13C), and [Li(THF)3{Si(SiPh3)3}], (7Li, 29Si).

The structure of lithium hexamethyldisilazide in the presence of OP(NMe2)3 has been investigated by 6Li, 15N, and 31P NMR spectroscopy, including 6Li-15N and 31P-6Li heteronuclear multiple quantum correlation spectroscopy. 23Na chemical shift calculations of Na- have been performed. 23Na NMR spectra of Na+ in ordered biological systems have been reported. 23Na NMR spectroscopy has been used to evaluate human erythrocyte Na+/K+/Cl- co-transport. Double quantum 23Na NMR studies of the halotolerant Ba1 bacterium have been reported. The complexation of Cs+ by mixed crown ethers has been investigated by 133Cs NMR spectroscopy. Caesium bonding in calix[4]arene systems has been investigated by 133Cs and 133Cs-1H HOESY NMR spectroscopy. NMR data have also been reported for [MeC{CH2N(Li)R}3]3, (7Li, 13C), [{LiNa[N(CH2Ph)2]2(OEt2)2}2], (7Li), 7, (13C), [Li(benzotriazole)(DMSO)], (13C), [Li(THF)2(μ-NHBut)2GaCy2], [MgCl(THF)2 (μ-3,5-Me2pz)2GaCy2], (13C), [HC{SiMe2N(Li)But}3], (7Li, 13C, 29Si), [Ph2P(N -SiMe3)2Li(THF)2], [{Ph2P(NSiMe3)2}2M]-, (M = Na, Cs; 6Li, 23Na, 29Si), [(Me3Si) -{(Me3Si)3Si}NLi]2, (7Li, 29Si), [Li{(2-NC5H4)2P}(THF)]2, (7Li), [Li(Ph4P2N4S2Ph)(THF)]2, (7Li), [(2-NMe2C6H4BMe3)Li(OEt2)], (7Li, 13C), [Li2(C6H12O2)2 {[3,4,5-(MeO)3C6H2]4-porphyrin}], (1Li), [Ph3PCHRCHR'OLi(THF)3], (6Li, 13C, 17O), [Li(DME)2I], (13C), [(PriOH)2K(μ-OPri)2Al(μ-OPri)2]n. (13C), [K(18-crown-6)][Ph2PCHC(O)Ph], (13C), Li+ salts of thiophosphamides, (6Li-1H HOESY, 7Li, 13C, [Li(THF)Se-2,4,6-But3C6H2]3, [Me3SiCH2-Zn Se-2,4,6-But3C6H2]3, (77Se), [(THF)2LiTeSi (SiMe3)3], (77Se, 125Te), and [Li{[(Me3Si)3Si]3Te}]6, (13C, 29Si).

The magnetic moment of 23Mg has been determined. NMR data have also been reported for [HB(3-Butpz)3BeMe], (9Be, 13C), 8, (R = 1-adamantyl, M = MgEt2, ZnEt2, AlH3; 13C, 15N), 9, (13C, including CPMAS), [Mg(1,8-naphthyl)]n. (13C), [{(η5-C5H5)Ti} {(η5-C5H5)Mg} {μ-η2, η2-C2(SiMe3)2}2], (13C), [{(η5-C5H5)Ti} {(η5-C5H5)Mg} (PMDETA)], (13C), [(η5-1,2,4-Pri3C5H2)2M], (M = Ca, Sr, Ba; 13C), [Ca2(OSiPh3)4(NH3)4], (13C, 29Si), [Ba(OSiPh2O-SiPh2O)(OH2)(NH3)0.33], (13C, 29Si), 10, (29Si), [Ba(hfac)(Me2NCH2CH2NMeCH2CH2-NMeCH2CH2NMe2)], [{(dpm)3Y}2(triglyme)], (13C, [Ba{HB(3,5-Me2Pz)3}2], (13C), [Ba{PhC(NSiMe3)2}2], (13C, 29Si), [Ba6(OPh)12(TMEDA)4], (13C), [Ba{R1COCHC-(NR2)R3)2], (13C), [M{P(SiMe3)2}2L4], (M = Ca, Ba; 13C, 15N, 29Si), [Ba{P(SiMe3)2}2 -(THF)2]n, (13C, 29Si), [Be6(OCH2CO2)8]4-, (9Be), [Be(OC6H4-2-CO2)2]2-, (9Be, 13C, magnesium salicylate, (13C), BaII, CaII, and SrII complexes with cryptand [2.2.2], AlIII, InIII, GaIII complexes with nonamethylimido diphosphoramide, (13C,3 CaII, SrII, BaIII, complexes of some tetralactams, (13C), [Ca(dpm)2(triglyme)], (13C), [Sr(dpm)2], (13C), [Sr(dpm)2{Me(OCH2-CH2)3OMe}], (13C), [Sr3 (dpm)6(dpmH)], [Ba4(dpm)8], (13C), [H2Sr6Ba2 (μ5-O)2 (OPh)14-(HMPA)6], (13C), [Ba(dpm)2(diglyme)2, (13C, [Ba(dpm)2(tetraglyme)], (13C), and [Y2Ba{OCH(CF3)2}4(dpm)4], (13C).

Complexes of Group 3, the Lanthanides, and Actinides. — The quadrupole moment of 41Sc has been measured by use of a modified β-NMR technique. The 13C NMR spectrum of 11 shows 1J(13C13C) = 80 Hz for the central olefin. 12 has been proposed as a relaxation reagent for 89Y NMR spectroscopy and applied to [Y{O2CCH2N[CH2CH2N(CH2CO2)2]2)]2-. It has been proposed that rare earth elements can be determined in mixtures by 1H and 13C NMR spectroscopy. NMR data have also been reported for [(η5-C5CH2CH2OMe)2YAlH4], (13C), [(η5-C5Me5)2 Y-(μ-H)(μ-η1, η5-CH2C5Me4) Y(η5-C5Me5)], (13C), [{(η5-C5H5)2NbH2}2Yb(diglyme)], [{(Me3P)5WH5}2 Yb(diglyme)], (13C, 171Yb), [(octaethylporphyrin)ScR], (R = Me, CH(SiMe3)2, η5-indenyl; 13C), [(η5-ButC5H4)2Y(η-Me)]2, (13C), [{(ButO)(THF)Y}(μ-OBut)(μ-Me)-AlMe2], (13C, and 89Y CP MAS), [(η5-C5H4SiMe3) Y{(μ-OBut)(μ-Me)AlMe2}2], (13C), [{PhC(NSiMe3)2}2YCH(SiMe3)2], (13C), [Li(THF)2 ({μ-η2:η8-C8H8}M {CH(SiMe3)3}2)2], (M = Y, Sm, Lu; 13C), 13, (13C, 171Yb), [Li(dioxan)1.5][La(η3-C3H5)4], (13C), [MeN(CH2-CH2C5H4-η5)2 YCl]2, (13C), [(η5-C5Me4H)3La], (13C), [(η5-C5H4CH2CH2NMe2)3La], (139La), [(η5-C5Me5)2La{O(CH2)4C5Me5} (THF)], (13C, including 13C-1H COSY), [(η8-C8H8) (η5-C5Me4H)M], (M = Y, La, Sm, Lu; 13C), [{(η5-C5Me5)Sm}2 {μ-η3:η3-1,2,3,4-(C5H4N)4C4H4}], (13C), [([etas]5-C5Me5)2Sm{C5H3(CH2NMe2)-η5} Fe(η5-C5H5)], (13C), [(η5-C5H4CH2CH2OMe)3Sm], (13C), [(η5-C5H4Me)2 (THF)Sm(μ-Cl)2, (13C), [(η5-C5H4Me)3-Yb], (13C), [Yb{η5-1,5-(Me3Si)2C5H5}2(diglyme)], (13C), [(η8-C8H8)M(OSiPh3){THF)], (M = Y, Lu; 13C), [{(Me3Si)2N}2Sm {μ-(η8:η8-C8H8)} Sm{N(SiMe3)2}2], (13C), 14, (13C), [(2,5-But2C4H2N)2M(THF)], (M = Sm, Yb; 13C), lanthanide complexes of 2-acetylpyridine-2-thenoylhydrazone, (13C), and 2,6-diacetylpyridine bis(2-pyridylhydrazone), (13C), [Lu{(Ph2P)2CH}3 (THF)], (13C), [ScCl2(15-crown-5)]+, (13C), [Y4(acac)10(OH)2], (89Y), [Y(dpm)3], (13C, 89Y), [Y{OCMe(CF3)2}3(THF)3], (89Y), [Cl2Y{Al(OPri)4}], (13C, 27Al, 89Y), 15, (13C), [La(dpm)3(tetraglyme)], (13C), [M(NO2)3 (HMPA)3], (M = La, Pr-Sm; 14N), [La2Na3 (μ4-OC6H4Me-4)3 (μ-OOC6H4Me-4)6(THF)5], (13C), [{(PriO)4Al} Sm-{Zr2 (OPri)9)2], (13C), [La(TeSi(SiMe3)3}3], (13C, 125Te), 16, (13C), and complexes of UO2 (NO3)2 with octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide, (13C).

(Continues...)

Excerpted from Spectroscopic Properties of Inorganic and Organometallic Compounds Volume 27 by G. Davidson. Copyright � 1994 The Royal Society of Chemistry. Excerpted by permission of The Royal Society of Chemistry.
All rights reserved. No part of this excerpt may be reproduced or reprinted without permission in writing from the publisher.
Excerpts are provided by Dial-A-Book Inc. solely for the personal use of visitors to this web site.

��ber diesen Titel� kann sich auf eine andere Ausgabe dieses Titels beziehen.

Anbieterinformationen

Hello! Ria Christie Collections is an online venture that was initially set up in 2012 to sell books. We do not have a physical high street store. We are professional online booksellers. We only sell brand new books in perfect condition that we source from various suppliers and the publishers. Primarily, our aim is to provide an excellent service to all our customers. We always work as a team to achieve this. Our other objectives are to: 1. Ensure that all our products reach their destination quickly in a safe and secure manner 2. Answer to all our customer queries within 24 hours 3. Ensure that our customers are happy with their purchases 4. Provide all the items at a competitive price 5. Always listen to our customers Ria Christie Collections is not a registered company. It is a Sole Trader venture. Other key information is shown below: Contact Person Name: Rakesh Luchmun (Mr) Storefront Name: Ria Christie Collections Place of Establishment Address: Suite B; ARUN House; ARUN Building Arundel Road Uxbridge UB8 2RR United Kingdom E-Mail Address: riachristie@hotmail.co.uk VAT Number: GB 160 5650 25 We always work hard and aim to comply with all of Abebooks Policies. If you have any issues, please do not hesitate to write to us whether before or after a purchase. We promise to reply to you promptly and, in any case, within 24 hours. Thank you kindly! Yours sincerely Mr Rakesh Luchmun (Founder) and the Ria Christie Collections Team

Zur Homepage des Verk�ufers

Unternehmensdaten des Verk�ufers

Ryefield Investments Limited
175 Pield Heath Road, Uxbridge, UB8 3NL, United Kingdom

Gesch�ftsbedingungen und Versandinformationen

Verkaufsbedingungen

All Returns and Refund are as per Abebooks policies.

Widerrufsbelehrung

Versandbedingungen

Orders usually ship within 2 business days. If your book order is heavy or oversized, we may contact you to let you know extra shipping is required. Thank you!

Versandkosten von Vereinigtes K�nigreich nach USA

Versandkosten von Vereinigtes K�nigreich nach USA
Bestellmenge	6 bis 12�Werktage	6 bis 12�Werktage
Erster Artikel	EUR 13.78	EUR 13.78

Die Versandzeiten werden von den Verk�uferinnen und Verk�ufern festgelegt. Sie variieren je nach Versanddienstleister und Standort. Sendungen, die den Zoll passieren, k�nnen Verz�gerungen unterliegen. Eventuell anfallende Abgaben oder Geb�hren sind von der K�uferin bzw. dem K�ufer zu tragen. Die Verk�uferin bzw. der Verk�ufer kann Sie bez�glich zus�tzlicher Versandkosten kontaktieren, um einen m�glichen Anstieg der Versandkosten f�r Ihre Artikel auszugleichen.