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-4 M in dichloromethane (Figures S9-S12, Supporting Information), and little change was observed with the band shape and extinction coefficient, indicating minimal intermolecular aggregation occurred under such conditions.
-
-4 M in dichloromethane (Figures S9-S12, Supporting Information), and little change was observed with the band shape and extinction coefficient, indicating minimal intermolecular aggregation occurred under such conditions.
-
-
-
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45
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68149086805
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For PEP and PEPEP due to significant overlap of the first and second reductive waves, deconvolution and accurate determination of the half-wave potentials were difficult; these values were estimated from the approximate peak position based on our best judgement and may thus present large errors, but the increasing trend relative to the value of PDI was evident.
-
For PEP and PEPEP due to significant overlap of the first and second reductive waves, deconvolution and accurate determination of the half-wave potentials were difficult; these values were estimated from the approximate peak position based on our best judgement and may thus present large errors, but the increasing trend relative to the value of PDI was evident.
-
-
-
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46
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0034618527
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In this review electronic coupling through phenylene groups was shown to be weaker than that through ethynylene units in ferrocene-related systems
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Barlow, S.1
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47
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2 and PEPEP.
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2 and PEPEP.
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