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D splitting

Protons of substrueture B and C are assigned by means of the mesomerie effeet of the aldehyde group whieh deshields the protons in o-position of the attaehed p-disubstituted benzenoid ring and in p-position of the eentral CC double bond ort/io-protons of the monosubstituted benzenoid ring D split into a doublet beeause of one ortho eoupling ( 7.5 Hz) while the meta-protons split into a triplet beeause of two ortho eouplings. [Pg.185]

All four heuristics are in conflict here. Heuristic 1 suggests doing the D/E split last, whereas Heuristic 3 suggests it should be done first. Heuristic 2 suggests the A/B split first and Heuristic 4 the C/D split first. [Pg.213]

D. SPLIT COLUMN PLUS AN ALDEHYDE CONCENTRATING COLUMN... [Pg.246]

Magnitude op the d-d Splitting Parameter A for Different Metal Hexacarbonyls and Hexacyanides... [Pg.248]

The ether linkage (d) splits first. This provides products without methoxyl groups. [Pg.221]

FIGURE 5 Tube designs (a) same diameter, hairpins, which are the most common (b) small diameter, single pass (c) increasing diameter (d) split coils two small-diameter coils to one large. [Pg.543]

Figure 6.1 (D) splits the cooling step for ammonia condensation and also compresses recycle gas together with the makeup gas. This design is especially useful at synthesis pressures above 25 MPa (250 bar). At these pressures, a greater portion of the ammonia can be liquefied by cooling with cooling water... Figure 6.1 (D) splits the cooling step for ammonia condensation and also compresses recycle gas together with the makeup gas. This design is especially useful at synthesis pressures above 25 MPa (250 bar). At these pressures, a greater portion of the ammonia can be liquefied by cooling with cooling water...
Protons a and b split each other into a doublet and a septet, respectively (a typical isopropyl group pattern). Protons c and d split each other into a quartet and a triplet, respectively (a typical ethyl group pattern). [Pg.584]

The particular splitting pattern of the d orbitals in Figure 4.5 is characteristic of cubic (octahedral type) crystal fields. In the tetrahedral type, the gg and ordering would be reversed. In other symmetries, the d splitting is as shown in Figure 4.6. [Pg.194]

Now one might return to the task identification stage, but at a higher level of detail to consider the possibility of separator designs not necessarily constrained to atmospheric pressure. In this example, the. solution thermodynamics are such that the A/B split is favored by higher pressures and the C/D split is favored by lower pressures. In the best unintegrated case, the A/BC column is increased in pressure until just below where a more expensive reboiling utility would be required, w hile the ABC/D column is decreased in pressure until just... [Pg.32]

Here the ligand field is stronger (p. 134), the d -d splitting is larger, and an electron falls into a 3d orbital, leaving two unpaired spins instead of the... [Pg.535]

Fig. 11 a-d Pulse sequences and coherence transfer pathways for the 2D STMAS experiment a two-pulse sequence as described by Gan b amplitude modulated z-filter acquisition scheme c phase-modulated shifted-echo experiment d split-ti shifted-echo experiment. The values of k, k and k" are chosen to refocus the second-order quadrupolar broadening at the end of the period... [Pg.166]

Table II. One election 7 ° 3 d splittings calculated for sandwich systems... Table II. One election 7 ° 3 d splittings calculated for sandwich systems...
A germane attempt to rank adsorbate ligands in terms of their Cu d-d splitting when the cation (Cu ) is coordinated on a silica surface had earlier been made by Trouillet et ai, in a Cu/Si02 matrix. Trouillet and co-workers applied the rule of averaged environment to conclude that the order was ethylenediamine (en) > ammonia > water > silica (Si02). A series similar to this is obtained from the present study, but includes pyridine and acetone. Thus, from Table 2 and Figure 7, we can therefore conclude that it is possible to use IR spectroscopy to monitor ammonia in the environment. [Pg.150]

D Approximate chemical shift values for D. Splitting patterns and coupling constants are given in brackets. [Pg.205]

Since only particular kinds of orbitals lead to octahedral symmetry i. e., dx2 y2, dz2, s, px, py, pz so the dxy, dyz and dxz will be unaffected by the bonding as these orbitals are not involved in the bond formation. The D, splitting between T2g eg depends upon the strength of the ligands. [Pg.8]


See other pages where D splitting is mentioned: [Pg.134]    [Pg.419]    [Pg.419]    [Pg.47]    [Pg.239]    [Pg.1184]    [Pg.578]    [Pg.149]    [Pg.567]    [Pg.205]    [Pg.17]    [Pg.262]    [Pg.59]    [Pg.185]    [Pg.1173]    [Pg.2840]    [Pg.158]    [Pg.159]    [Pg.44]    [Pg.27]    [Pg.1175]    [Pg.1195]    [Pg.82]    [Pg.30]    [Pg.849]    [Pg.129]    [Pg.111]    [Pg.112]    [Pg.113]    [Pg.73]    [Pg.305]   
See also in sourсe #XX -- [ Pg.46 , Pg.276 ]




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Crystal field splitting of d orbitals

Crystal field theory d-orbital splitting in octahedral and tetrahedral complexes

Crystal-Field Splitting of Free-Ion D Terms

D orbitals splitting

D-orbital splitting

Interelectronic Repulsion and Ligand Field Splitting When There Is Ambiguity in the d-Electron Configuration

Ligands splitting d orbitals in an octahedral field

Octahedral crystal field splitting of d orbitals

Splitting d orbitals in an octahedral

Splitting d orbitals in an octahedral field of ligands

Splitting of d Orbital Energies in Octahedral Fields

Splitting of d Orbitals in Octahedral Symmetry

Splitting of d Orbitals in Tetrahedral and Other Symmetries

Splitting of d orbitals in the octahedral crystal field

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