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1 , despite the potential stabilization of the odd electron by two conjugated triple bonds and unlike t
2 o comprise increased relative amounts of the odd-electron c-type ions (c+*) and the even-electron z-t
3 led by a composite spin density map (SDM) of odd electron character on the electron density surface,
4 ly access various oxidation states including odd-electron configurations.
5 s the question of pi-delocalization in these odd-electron counterparts.
6 oubled" ESR spectrum diagnostic of complete (odd) electron delocalization.
7 Penning ionization with formation of radical odd-electron doubly charged molecular cation or via high
8 [triple bond]C units in conjugation with the odd electron enhances rather than diminishes stability.
9 up is the acid, (HPX-CO2H)FeIII(OH), because odd-electron homolytic O-O bond cleavage is inhibited.
10              Moreover, the delocalization of odd electrons in these radicals has been investigated by
11 S/MS), but unlike CFM-ESI, CFM-EI can handle odd-electron ions and isotopes and incorporates an artif
12            DFT calculations suggest that the odd electron is localized in a smif pi* orbital, i.e., s
13 d a series of b- and y-type ions; CID of the odd-electron Lbeta11(*) product resulted in a wide range
14 rison between the gas-phase fragmentation of odd-electron M+*, [M + H]2+*, and [M - 2H]-* ions of mod
15 lyzed reactions are proposed to also involve odd-electron Ni(I) and Ni(III) oxidation states.
16 CN, CO2Me, CHO, C3HMeBF2O2, and NO2 when the odd electron of the intervalence oxidation level is remo
17 o-9-azabicyclo[3.3.1], NPPh3, and O when the odd electron of the intervalence oxidation level is remo
18 ation in the C-C-O-C fragment brings the two odd-electron orbitals closer to each other, and the othe
19 derstanding of the fragmentation patterns of odd-electron peptide ions produced through various appro
20 lay an important role in the dissociation of odd-electron peptide ions.
21 cleavages are observed, as well as even- and odd-electron products.
22                                      Unusual odd-electron radical a- and x-ions were observed.
23 on product ion termed Lalpha12, the other an odd-electron radical ion termed Lbeta11(*), which allowe
24 By increasing the field strength about iron, odd-electron reactivity was circumvented via increased c
25 hese reactions occur in place of undesirable odd-electron redox processes that produce hydroxyl radic
26                                              Odd-electron, redox-active ligands are discussed in the
27 idation of Fe(II) by H(2)O(2), thus avoiding odd electron reduction products of oxygen and therefore
28 roton and (13)C spin densities show that the odd electron resides in a molecular orbital with six hyd
29   In the reduced monomer's ground state, the odd electron resides on the dmb ligand rather than on th
30                                              Odd-electron silver clusters are found to be especially
31  it is in agreement with the distribution of odd-electron spin electron density from the ESR data and
32 n even electron systems and rapid etching in odd electron systems.
33                      The EPR spectrum of the odd-electron Y2@C79N indicates that the spin density lar
34                      Here we report that the odd electron z (*) -type ions formed by the electron-bas
35 involves production and isolation of primary odd-electron z(*) ions, followed by radical site initiat

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