US2007194277A1PendingUtilityA1
Light emitting polymer
Est. expiryJun 29, 2021(expired)· nominal 20-yr term from priority
H10K 59/8793H10K 85/141C07D 285/14C09K 2211/1425G02F 1/133603C08G 61/122C09K 11/06C09K 19/3497C09K 19/32G02F 1/13362C08G 61/12C08G 61/02C09K 2019/0448C09K 2211/1458C07D 333/08C09K 2211/1416C09K 19/60C09K 19/38C09B 69/109C09K 2211/1483C09B 69/103C09K 19/3861H10K 50/11H10K 50/14H10K 85/633H10K 85/115H10K 85/113H10K 85/6565H10K 50/868
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Claims
Abstract
There is provided a process for forming a light emitting polymer comprising photopolymerization of a reactive mesogen having an endgroup which is susceptible to photopolymerization e.g. by a radical polymerization process. Also provided are methods for using the light emitter in displays, backlights, electronic apparatus and security viewers.
Claims
exact text as granted — not AI-modified1 . A light emitting or charge transporting polymer comprising a polymer formed from reactive mesogens having the formula:
B—S-A-S—B●
wherein
A is a chromophore of general formula —(Ar-Fl) n -Ar—
wherein
Ar is an aromatic diradical or a heteroaromatic diradical bonded linearly or substantially linearly to adjoining diradicals, or a single bond;
Fl is a 9,9-dialkyl substituted fluorene diradical joined to adjoining diradicals at the 2 and 7 positions;
the Ar and Fl diradicals may be chosen independently in each of the n subunits of the chromophore; and
1≦n≦10,
S is a spacer;
B is an unradicalised endgroup which is susceptible to polymerization; and
B● is a radicalised endgroup.
2 . The polymer of claim 1 , wherein the B● radicalised endgroup is able to react with the unradicalised endgroup (B) to form a cyclic entity.
3 . The polymer of claim 2 , wherein the reaction of the B● radicalised endgroup with the unradicalised endgroup (B) is susceptible to steric control.
4 . The polymer of claim 1 , wherein the unradicalised endgroup B is susceptible to photopolymerization.
5 . The polymer of claim 4 , wherein the polymer is formed by photopolymerization.
6 . The polymer of claim 1 , wherein the unradicalised endgroup (B) comprises a diene.
7 . The polymer of claim 6 , wherein the diene is selected from the group consisting of 1,4 dienes, 1,5 dienes and 1,6 dienes.
8 . The polymer of claim 6 , wherein the diene functionalities are separated by an aliphatic linkage.
9 . The polymer of claim 6 , wherein the diene functionalities are separated by an inert linkage.
10 . The polymer of claim 9 , wherein inert linkage is selected from the group consisting of ether and amine linkages.
11 . The polymer of claim 1 , wherein the light emitting or charge transporting polymer is a light emitting electroluminescent polymer.
12 . The polymer of claim 1 , wherein light emitting or charge transporting polymer is a hole transporting polymer.
13 . The polymer of claim 1 , wherein the light emitting or charge transporting polymer is an electron transporting polymer.
14 . The polymer of claim 1 , wherein the light emitting or charge transporting polymer is substantially photoinititor free.
15 . The polymer of claim 1 , wherein 2≦n≦7.Join the waitlist — get patent alerts
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