Symmetrical bridging

Hydrogen atoms chemisorbed on a metal surface may be bonded to just one metal atom or may be bonded to two atoms in a symmetrical bridge. In each case, there are three normal modes. Sketch what these are, and indicate any degeneracies (assume the metal atoms to be infinitely heavy). [Pg.742]

As mentioned, we also carried out IR studies (a fast vibrational spectroscopy) early in our work on carbocations. In our studies of the norbornyl cation we obtained Raman spectra as well, although at the time it was not possible to theoretically calculate the spectra. Comparison with model compounds (the 2-norbornyl system and nortri-cyclane, respectively) indicated the symmetrical, bridged nature of the ion. In recent years, Sunko and Schleyer were able, using the since-developed Fourier transform-infrared (FT-IR) method, to obtain the spectrum of the norbornyl cation and to compare it with the theoretically calculated one. Again, it was rewarding that their data were in excellent accord with our earlier work. [Pg.143]

These results, which pertain to stable-ion conditions, provide strong evidence that foe most stable structure for foe norbomyl cation is foe symmetrically bridged nonclassical ion. How much stabilization does foe a bridging provide An estimate based on molecular mechanics calculations and a foermodynamic cycle suggests a stabilization of about 6 1 kcal/mol. An experimental value based on mass-spectrometric measurements is 11 kcal/mol. Gas-phase Itydride affinity and chloride affinity data also show foe norbomyl cation to be especially stable. ... [Pg.330]

Again, the chloride is almost exclusively the exo isomer. The distribution of deuterium in the product was determined by NMR spectroscopy. The fact that 1 and 2 are formed in unequal amoimts excludes the symmetrical bridged ion as the only intermediate. The excess of 1 over 2 indicates fliat some syn addition occurs by ion-pair collapse before the bridged ion achieves symmetry with respect to the chloride ion. If the amount of 2 is taken as an indication of the extent of bridged-ion involvement, one would conclude that 82% of the reaction proceeds through this intermediate, which must give equal amoimts of 1 and 2. [Pg.358]

It is possible that a sixth (symmetrical bridging) mode M—O O—M occurs in... [Pg.464]

Similarly, when both the Cp and arene ligands are permethylated, the reaction of 02 with the Fe1 complex leads to C-H activation of the more acidic benzyl bond [57]. When no benzylic hydrogen is present, superoxide reacts as a nucleophile and adds onto the benzene ligand of the FeCp(arene)+ cation to give a peroxocyclohexadienyl radical which couples with a Fe Cp(arene) radical. A symmetrical bridging peroxo complex [(Fe"Cp)2(r 5-C6H60)2] is obtained. The C-H activation reactions of the 19e Fe1 radicals BH can be summarized as follows... [Pg.60]

A structural variation shows the borido cluster d HFe4(CO),2(Et3PAu)2B, where the B atom is within bonding contact of all six metal atoms and the two Au atoms symmetrically bridge the wingtips of the butterfly-shaped complex ... [Pg.49]

Knowing the values of all other parameters, we thus can find the cell s impedance. When a symmetric bridge is used (where the values of impedance in the third and fourth arms are identical), the unknown ceU impedance components will be equal to the values of R 2 nd 2 or R 2 and 2 in the second bridge arm. [Pg.210]

The range of structural alternatives explored by valency-deficient carbon species and the subtle interplay of substituents is remarkable. Scheme 7.6 (ORTEP adapted from reference 31) illustrates an example of an X-ray structure clearly describing a localized [C-H C+] carbenium ion (A) where a symmetric bridging structure [C-H-C] + (B) could have been assumed. In this case it is proposed that a charge-transfer interaction between the resonance delocalized cation and the adjacent electron-rich carbazol moiety may be responsible for the stabilization of the localized form over the three-center, two-electron (3c-2e) bridging structure. [Pg.283]

Trifluorophosphane can behave as a /x3 donor towards a triangular palladium core.559,360 The symmetrically bridging / -coordination mode has little precedent for tertiary ligands based on Group 15 atoms. The synthesis of a Pd1 dimer featuring a strongly bonded symmetrically bridging /i2-phosphole unit, which is the first example of this coordination mode for a tertiary phosphane, has been reported.561... [Pg.603]

Old semi-empirical (Bach and Henneike, 1970) and recent ab initio (Hamilton and Schaefer, 1990, 1991) calculations are in complete agreement with experimental data as regards the structure of the parent ethylene-bromonium ion. Its most stable structure is definitely symmetrically bridged. Early ab initio results showed that the bridged form [7] is more stable than the 2-bromoethylcation [8] and the 1-bromoethylcation [9] by 1-4 and... [Pg.224]

Bicycloalkylidenes. a-Delocalization in bicyclic carbocations provides the opportunity to detect the protonation of bicycloalkylidenes. An obvious choice was the 2-norbomyl cation (66), for which symmetrical bridging (equivalence... [Pg.9]

As in main-group chemistry, hypovalent hydrides of the transition series have pronounced tendencies to form bridging tau bonds. In addition to H4TaTaH4, the multiply bonded species HTaTaH features two symmetrically bridging hydrides. Despite the complexity introduced by such tau bonds, the Ta-Ta interaction clearly has high bond order, as simple Lewis-like structures prescribe. [Pg.415]

In fact, the barrier for proton transfer in the maleate anion appears to lie below the zero-point vibrational energy level (W. M. Westler, private communication). Thus, vibrationally averaged properties of the maleate anion will correspond to a symmetrically bridged Cjv transition-state structure rather than to either of the asymmetrically bridged equilibrium structures in Fig. 5.22. For present purposes this interesting feature of the potential surface can be ignored. [Pg.706]

The structure of the 2-norbornyl cation has been a focal point of controversy in physical organic chemistry. Experimental NMR spectroscopy and computational methods have been the decisive tools, favoring the hypercoordinated symmetric bridged structure 30, a protonated nortricyclane.79 The tricoordinated 2-norbornyl cation 31 is not a local minimum (MP2/6-31G(d)) on the energy surface.80... [Pg.148]

Similarly to the 2-norbornyl cation, comparison of calculated (IGLO/DZ//MP2/ 6-31G(d)) and experimental 13C NMR chemical shifts allowed to differentiate between the hypercoordinated 70 and the trivalent form 71 of the bicyclo[2.1.1.]hexyl cation.85 The experimental (157.8 ppm) and calculated (158.5 ppm) values for Cl and C2 (averaged signal) are reported to be nearly identical for the symmetrically bridged... [Pg.149]

Chiral, Ci-symmetric (asymmetric) bridged metallocenes, 16 108-109 Chiral, C2-symmetric bridged metallocenes, 16 104-108 Chiral, C2-symmetric catalysts, racemic mixture of, 16 106 Chiral, C2-symmetric unbridged metallocenes, 16 108 Chiral catalysts, 16 395 Chiral centers, in biochemical compounds, 17 402... [Pg.173]

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