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Doublet-triplet

Monomer (Section 6 21) The simplest stable molecule from which a particular polymer may be prepared Monosaccharide (Section 25 1) A carbohydrate that cannot be hydrolyzed further to yield a simpler carbohydrate Monosubstituted alkene (Section 5 6) An alkene of the type RCH=CH2 in which there is only one carbon directly bonded to the carbons of the double bond Multiplicity (Section 13 7) The number of peaks into which a signal IS split in nuclear magnetic resonance spectroscopy Signals are described as singlets doublets triplets and so on according to the number of peaks into which they are split... [Pg.1289]

Multiplicity (Section 13.7) The number of peaks into which a signal is split in nuclear magnetic resonance spectroscopy. Signals are described as singlets, doublets, triplets, and so on, according to the number of peaks into which they are split. [Pg.1289]

Singlet. Doublet. Triplet. Shifts in p.p.m. from external TFA + upheld from TFA. Coupling constants in Hertz. Basic quartet, C1F5 group CF, 6.76, multiplet CFj, 38.4, J TF = 3.3, septet. Triplet. 4 of 10 lines. Pentet. Septet. Quartet. 6 of 8 lines. 7 of 9 lines. Septet. Quartet. Triplet. 5 of 7 lines. Sextet. " Pentet. 6 of 8 lines. Pentet. Quartet. Pentet. Sextet. Sextet. Doublet. 5 of 7 lines. " Pentet. Pentet. Quartet. Pentet. Quartet. Triplet. Triplet. Triplet. [Pg.199]

Singlet. Doublet. Triplet." Chemicalshiftsinp.p.m. + downfield from external MciSi. Coupling constants in Hertz. " OH (2.43), singlet. [Pg.200]

Doublet. Triplet. Not recorded. Shifts in p.p.m. from external TEA, + upheld from TEA. Coupling constants in Hertz. Jff = 1.4 (triplet). = 1.5 (multiplet),... [Pg.202]

The SMO can be extended to the overlap probabilities of 2D spots. Davis and coworkers (Davis, 1991 Oros and Davis, 1992) determined the number of singlets, doublets, triplets, and total number of spots as... [Pg.73]

H4WNH3 — H3WNH3 — h2wnh3 singlet doublet triplet... [Pg.446]

Generally, splitting of NMR signals to multiplets (doublet, triplet, quartet) is found for compounds containing two or more adjacent sets of unequivalent protons. But no multiplet structure of signals is observed when non-equivalent protons are separated by a proton free atom as seen in case of ter. butylamine. [Pg.255]

What causes NMR peaks to be split into doublets, triplets, etc. How does the presence of split peaks assist with qualitative analysis ... [Pg.295]

In 1925, Wolfgang Pauli gave chemists what they wanted from the physicists a physical principle underlying electron-pair valency. Pauli built on the fact that in addition to the continuous, line, and band spectra, there is a fine structure of doublets, triplets, and multiple lines, some of which are split in a magnetic field (Zeeman effect). [Pg.248]

Spin-restricted procedures, signified by an R prefix (e.g. RHF, RMP), constrain the a and (3 orbitals to be the same. As such, the resulting wavefunctions are eigenfunctions of the spin-squared operator (S2) that correspond to pure spin states (doublets, triplets, etc). The disadvantage of this approach is that it restricts the flexibility in the... [Pg.162]

In order to find out if the decomposition of NaAlH destabilizes the MgH constituent in a composite, the peak temperatures of the last peak in a doublet/triplet in Fig. 3.38b-d which supposedly corresponds to the decomposition of MgH are plotted as a function of vol.%NaAlH in Fig. 3.39. It is quite clear that the ROM behavior for the MgH temperature is not obeyed for this composite system in contrast to the (MgH + LiAlH ) composite system. There are two factors which may be responsible for this behavior. [Pg.269]

The different types (doublet, triplet, and so on) exhibit a characteristic ratio of intensities. Doublets are equally intense. Triplets have a more intense central peak flanked by two equal peaks of lesser intensity. A quartet has two equally intense central peaks with two smaller outer peaks that are equal to each other in intensity. See Figure 5-4 for the NMR spectrum of ethanol. [Pg.76]

Afterward, we have to find approximations for 2-RDM spin components D". Let us now focus on high-spin cases only, such as doublet, triplet, quartet... spins for one, two, three. .. unpaired electrons outside the closed shells. Accordingly, singly occupied orbitals will always have the same spin (Al p = 0 or = 0) so the trace of the one-matrix, Eq. (6), becomes... [Pg.414]

The integrated difference of majority and minority spin electronic charges, denoted by M, is given in column 3 of Table 4. The spectroscopic multiplicity of the complex is M +1. We see that for MA complexes Au O with even (odd) n, that is, with odd (even) number of electrons, the minimum energy isomer is a doublet (triplet). These M +l values coincide with the ones found by Yoon and coworkers , except for 4c and 7b structures, where these authors obtained M =3 and M =2, respectively. Note that these two cases are the only MA complexes with significant different values compared to our results. [Pg.425]

The reaction with 4-hydroxy-TEMPO leading to the ether is particularly interesting as the reaction could be spin allowed (i.e., doublet - - triplet —> doublet) if sufficient interaction between the O—H and nitroxide centers takes place. However, the EPR parameters for 4-hydroxy-TEMPO suggest that the interaction between the two sites is small.The magnitude of the relaxation of spin conservation rules seems unclear, but the kinetic results show virtually no effect. The rate constant for insertion at the O—H bond is 2 x 10 s, which is essentially the... [Pg.430]

FINE STRUCTl RF In atomic spectra, the occurrence of a spcclr.ll line us a doublet, triplet, etc., due to the interaction or coupling between the orbital angular momentum and the spin angular momentum olThe electrons in the emitting atoms. Fine structure is also exhibited by spectra nf particles. See also Atomic Spectra. [Pg.636]

The dynamic state is defined by the values of certain observables associated with orbilal and spin motions of the electrons and with vibration and rotation of [lie nuclei, and also by symmetry properties of the corresponding stationary-state wave functions. Except when heavy nuclei ate present, the total electron spin angular momentum of a molecule is separately conserved with magnitude Sh. and molecular slates are classified as singlet, doublet, triplet., . according to the value of the multiplicity (25 + I). This is shown by a prefix superscript lo the term symbol, as in atoms. [Pg.1037]

Note any obvious splitting of the absorptions in the table (e.g. doublet, triplet, quartet, etc.). For spectra which appear to show first-order splitting, the coupling constants of each multiplet should be determined by measuring the separation between adjacent peaks in the multiplet. Any other recognisable patterns which are not first order should be noted. [Pg.360]

The numbers 1, 2, 3, 4, etc., represent the maximum multiplicities in the spectral terms or atomic energy levels belonging to the corresponding systems of spectral structures, singlets, doublets, triplets, quartets, etc. Those in parentheses, still unknown, are suggested from considerations of symmetry. [Pg.8]


See other pages where Doublet-triplet is mentioned: [Pg.1134]    [Pg.120]    [Pg.120]    [Pg.224]    [Pg.224]    [Pg.9]    [Pg.261]    [Pg.237]    [Pg.201]    [Pg.31]    [Pg.147]    [Pg.511]    [Pg.469]    [Pg.11]    [Pg.128]    [Pg.257]    [Pg.286]    [Pg.218]    [Pg.63]    [Pg.201]    [Pg.101]    [Pg.34]    [Pg.14]    [Pg.224]    [Pg.224]    [Pg.170]    [Pg.814]    [Pg.94]    [Pg.226]   
See also in sourсe #XX -- [ Pg.508 ]




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