1988
DOI: 10.1021/ja00211a055
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Electronic properties of phosphazene substituents on ferrocene

Abstract: Crystal data and crystallographic data for (la)6-Li2O(thf)10 and tables of atomic positional and thermal parameters and bond distances and angles (9 pages); tables of observed and calculated structure factors (23 pages). Ordering information is given on any current masthead page.

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Cited by 39 publications
(13 citation statements)
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“…The values are on the order of 10 À3 cm s À1 .T he reaction rates of the RINs in this study are greater than those of the active materials in Zn/Br 2 and all-vanadium batteries. In addition, the modification of the ligand (i.e.,P hen) by electron withdrawing substituents, [44,45] We couldo bserve FE dissociation ath igher concentration to confirm the effect of concentration on the dissociation. The rapid response at a4Cr ate and good cycle life are attributed to the large rate constants and reversible behavior of the RINs.…”
Section: Diffusion Coefficients and Heterogeneous Electron-transfer Rmentioning
confidence: 77%
See 1 more Smart Citation
“…The values are on the order of 10 À3 cm s À1 .T he reaction rates of the RINs in this study are greater than those of the active materials in Zn/Br 2 and all-vanadium batteries. In addition, the modification of the ligand (i.e.,P hen) by electron withdrawing substituents, [44,45] We couldo bserve FE dissociation ath igher concentration to confirm the effect of concentration on the dissociation. The rapid response at a4Cr ate and good cycle life are attributed to the large rate constants and reversible behavior of the RINs.…”
Section: Diffusion Coefficients and Heterogeneous Electron-transfer Rmentioning
confidence: 77%
“…Low potentialo utput by the dissociation of FE can be improved by using milder electrolytes than the 1.0 m H 2 SO 4 solution used in this study.F Ed issociation is less in milder electrolytes. In addition, the modification of the ligand (i.e.,P hen) by electron withdrawing substituents, [44,45] We couldo bserve FE dissociation ath igher concentration to confirm the effect of concentration on the dissociation. Figures S5 Aa nd S5 Bs how the cyclet est with two to three times the concentration of the active materials that we used to obtain Figure 5.…”
Section: Diffusion Coefficients and Heterogeneous Electron-transfer Rmentioning
confidence: 77%
“…[14] Also, they have fairly good solubility in many organic solvents. [16,17] Transition-metal ions that coordinate with a pair of cyclopentadienyl anions can form various complexes, named metallocenes. Modification with functional groups can change the electrochemical properties of the redox pairs.…”
Section: Introductionmentioning
confidence: 99%
“…The electron-withdrawing or -donating properties of the functional groups can lead to redox potential shifts and changes in kinetics. [16,17] Transition-metal ions that coordinate with a pair of cyclopentadienyl anions can form various complexes, named metallocenes. By replacing metals or substituents on the cyclopentadienyl rings, numerous redox pairs can be formed, which can provide wide ranges of reaction rates and output potentials.…”
Section: Introductionmentioning
confidence: 99%
“…The electron withdrawing nature of cyclophosphazenes may account for this failure. 19 The standard enthalpy of formation of an energetic compound is a very important characteristic which can be calculated from heats of combustion using Hess thermochemical equations. The standard enthalpies of formation of the chlorophosphazene trimer and tetramer were reported as 2811.33 and 21083.03 kJ mol 21 , respectively.…”
mentioning
confidence: 99%