1984
DOI: 10.1039/c39840000204
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Corrigenda

Abstract: In Table 1, the room-temperature lifetimes for [ C u ( d ~p ) ~] + and [Cu(tpp)2]+ are incorrect and should be 240 and 190 ns, respectively. The quantum yields are also incorrect and should be as follows: [ C ~( d m p ) ~] + 2.1 x [ C ~( d p p ) ~] + 8.0 x [Cu(bcp)J+ 2.5 X and [ C ~( t p p ) ~] + 10.0 x

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Cited by 20 publications
(38 citation statements)
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“…When the interaction is strong, the lifetime of the MLCT state is shortened significantly and the luminescence is quenched, which has been characterized by the exciplex formation reported previously. [123][124][125][126][127] Therefore, the pump-probe XAFS measurements in the time domain provide new insights into the fundamental aspects of structural factors that may influence photoinduced electron and energy-transfer processes (Figure 11 b).…”
Section: Methodsmentioning
confidence: 99%
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“…When the interaction is strong, the lifetime of the MLCT state is shortened significantly and the luminescence is quenched, which has been characterized by the exciplex formation reported previously. [123][124][125][126][127] Therefore, the pump-probe XAFS measurements in the time domain provide new insights into the fundamental aspects of structural factors that may influence photoinduced electron and energy-transfer processes (Figure 11 b).…”
Section: Methodsmentioning
confidence: 99%
“…+ -the "Exciplex" [79,122] The MLCT excited states of cuprous diimine compounds are potential-energy and electron donors, [123][124][125][126][127][128] and functional moieties in molecular devices, because of their room temperature luminescence and structural reorganization upon Cu I -Cu II interconversion triggered electrochemically or photochemically. [129,130] Among these compounds, [Cu I (dmp) 2 ] + (dmp = 2,9-dimethyl-1,10-phenanthroline) is one of the most extensively studied, in which the photoinduced MLCT transition can be shown as, [Cu I (dmp) 2 ] + + hn!…”
Section: The Mlct State Structures Of Cu I (Dmp)mentioning
confidence: 99%
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“…One successful example of a lithium templated synthesis of [2]-catenanes by using metathesis has been reported previously. [33] We have explored the influence of Li-templated complexation on catenane formation in our system: as previously reported, catenanes 4 and 5 could be synthesized by using the reversible-alkene-metathesis reaction. [34] The yield obtained was in accordance with the strength of the donor-acceptor interactions giving a 20 % yield of 4 and 60 % yield for 5.…”
Section: In Memory Of Norma Stoddartmentioning
confidence: 99%