2007
DOI: 10.1002/anie.200605055
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New Crosslinkable Hole Conductors for Blue‐Phosphorescent Organic Light‐Emitting Diodes

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Cited by 154 publications
(132 citation statements)
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“…We emphasize that the findings we report here are general for oxetane-functionalized, cross-linkable materials, as verified by testing 20 different organic semiconductors including monomeric (x-MHTM) [26] and polymeric hole conductors (x-PHTM) [23] as well as cross-linkable emitting polymers (x-R, x-G, and x-B, see Supporting Information Fig. 1 for chemical structures).…”
mentioning
confidence: 58%
“…We emphasize that the findings we report here are general for oxetane-functionalized, cross-linkable materials, as verified by testing 20 different organic semiconductors including monomeric (x-MHTM) [26] and polymeric hole conductors (x-PHTM) [23] as well as cross-linkable emitting polymers (x-R, x-G, and x-B, see Supporting Information Fig. 1 for chemical structures).…”
mentioning
confidence: 58%
“…S1 and S6), which features a low highest occupied molecular orbital (HOMO) level [17] enabling space-charge-limited current (SCLC). The X-HTL also features a high hole mobility (m) of 3.5 Â 10 À4 cm 2 V À1 s À1 in trap-limited SCLC and a value of 10 À3 cm 2 V À1 s À1 for trap-free SCLC.…”
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confidence: 99%
“…In situ cross-linking reactions have also been explored to afford covalently bound structures that are highly resistant to processing solvents [11][12][13][14][15][16][17][18][19] . Despite their high mechanical robustness and compatibility with subsequent solution processing, polymers are plagued by limited reproducibility in the device performance because of batch-tobatch variations with respect to molecular weight, polydispersity, regioregularity and purity [20][21][22][23] .…”
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confidence: 99%