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Extract from the Register of European Patents

EP About this file: EP1431289

EP1431289 - Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds [Right-click to bookmark this link]
StatusNo opposition filed within time limit
Status updated on  08.11.2013
Database last updated on 24.04.2024
Most recent event   Tooltip08.11.2013No opposition filed within time limitpublished on 11.12.2013  [2013/50]
Applicant(s)For all designated states
E. I. du Pont de Nemours and Company
1007 Market Street
Wilmington, DE 19898 / US
[N/P]
Former [2013/01]For all designated states
E.I. DU PONT DE NEMOURS AND COMPANY
1007 Market Street
Wilmington, DE 19898 / US
Former [2004/26]For all designated states
E.I. DU PONT DE NEMOURS AND COMPANY
1007 Market Street
Wilmington, Delaware 19898 / US
Inventor(s)01 / Petrov, Viacheslav A.
2 Cappa Court
Hockessin DE 19707 / US
02 / Wang, Ying
4010 Greenmount Road
Wilmington DE 19810 / US
03 / Grushin, Vladimir
533 Runnymeade Road
Hockessin DE 19707 / US
 [2004/26]
Representative(s)Towler, Philip Dean
Dehns
St Bride's House
10 Salisbury Square
London EC4Y 8JD / GB
[N/P]
Former [2013/01]Towler, Philip Dean
Dehns St Bride's House 10 Salisbury Square London
EC4Y 8JD / GB
Former [2004/26]Towler, Philip Dean
Frank B. Dehn & Co., European Patent Attorneys, 179 Queen Victoria Street
London EC4V 4EL / GB
Application number, filing date04004543.727.06.2001
Priority number, dateUS20000215362P30.06.2000         Original published format: US 215362 P
US20000224273P10.08.2000         Original published format: US 224273 P
[2004/26]
Filing languageEN
Procedural languageEN
PublicationType: A2 Application without search report 
No.:EP1431289
Date:23.06.2004
Language:EN
[2004/26]
Type: A3 Search report 
No.:EP1431289
Date:24.12.2008
[2008/52]
Type: B1 Patent specification 
No.:EP1431289
Date:02.01.2013
Language:EN
[2013/01]
Search report(s)(Supplementary) European search report - dispatched on:EP24.11.2008
ClassificationIPC:H01L51/00, C09K11/06, H05B33/14, C07D213/30, C07F15/00, C07D213/61, C07D213/26, C07D213/68, C07D239/26, H01L51/30, C07D215/04
[2012/31]
CPC:
H05B33/14 (EP,US); C09K11/06 (EP,KR,US); C07D213/26 (EP,US);
C07D213/30 (EP,US); C07D213/61 (EP,US); C07D213/68 (EP,US);
C07D215/04 (EP,US); C07D239/26 (EP,US); C07F15/0033 (EP,US);
H10K85/341 (EP,US); H10K85/342 (EP,US); C09K2211/1007 (EP,US);
C09K2211/1011 (EP,US); C09K2211/1014 (EP,US); C09K2211/1029 (EP,US);
C09K2211/185 (EP,US); H10K50/00 (US); H10K50/11 (EP,US);
H10K85/60 (EP,US); Y10S428/917 (EP,US) (-)
Former IPC [2008/52]H05B33/14, C09K11/06, C07F15/00, C07D213/61, C07D213/26, C07D213/68, C07D239/26, H01L51/30
Former IPC [2004/26]C07D213/26, C07D213/61, C07D213/68, C07D239/26, C07F15/00, C09K11/06, H05B33/14, H01L51/30
Designated contracting statesDE,   GB [2009/36]
Former [2004/26]AT,  BE,  CH,  CY,  DE,  DK,  ES,  FI,  FR,  GB,  GR,  IE,  IT,  LI,  LU,  MC,  NL,  PT,  SE,  TR 
TitleGerman:Elektrolumineszente Iridiumverbindungen mit fluorierten Phenylpyridinen, Phenylpyridinen und Phenylchinolinen und solche Verbindungen enthaltende Vorrichtungen[2004/26]
English:Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds[2004/26]
French:Composés d'iridium électroluminescents contenant des phénylpyridines fluorées, des phénylpyrimidines et des phénylquinolines et dispositifs fabriqués avec ces composés[2004/26]
Examination procedure12.05.2009Examination requested  [2009/26]
25.06.2009Loss of particular rights, legal effect: designated state(s)
16.07.2009Despatch of a communication from the examining division (Time limit: M06)
03.08.2009Despatch of communication of loss of particular rights: designated state(s) AT, BE, CH, CY, DK, ES, FI, FR, GR, IE, IT, LU, MC, NL, PT, SE, TR
25.01.2010Reply to a communication from the examining division
23.01.2012Despatch of a communication from the examining division (Time limit: M04)
01.06.2012Reply to a communication from the examining division
20.08.2012Communication of intention to grant the patent
22.11.2012Fee for grant paid
22.11.2012Fee for publishing/printing paid
Parent application(s)   TooltipEP01950576.7  / EP1295514
Divisional application(s)The date of the Examining Division's first communication in respect of the earliest application for which a communication has been issued (EP20010950576) is  30.05.2003
Opposition(s)03.10.2013No opposition filed within time limit [2013/50]
Fees paidRenewal fee
27.02.2004Renewal fee patent year 03
01.07.2004Renewal fee patent year 04
14.06.2005Renewal fee patent year 05
14.06.2006Renewal fee patent year 06
14.06.2007Renewal fee patent year 07
28.03.2008Renewal fee patent year 08
16.06.2009Renewal fee patent year 09
11.06.2010Renewal fee patent year 10
13.06.2011Renewal fee patent year 11
31.03.2012Renewal fee patent year 12
Penalty fee
Additional fee for renewal fee
30.06.200404   M06   Fee paid on   02.09.2004
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Documents cited:Search[A]WO9603410  (BOEHRINGER MANNHEIM GMBH [DE], et al) [A] 1-11 * claims 1,2,20,21 *;
 CN1245822  [ ] (UNIV JILIN [CN]);
 [DA]  - DJUROVICH PETER I ET AL, "Ir(III) CYCLOMETALATED COMPLEXES AS EFFICIENT PHOSPHORESCENT EMITTERS IN POLYMER BLEND AND ORGANIC LEDs", POLYMER PREPRINTS, (2000), vol. 41, no. 1, pages 770 - 771, XP001052648 [DA] 1-11 * the whole document *
 [A]  - CHATANI N; IE Y; KAKIUCHI F; MURAI S, "Ru3(CO)12-Catalyzed Reaction of Pyridylbenzenes with Carbon Monoxide and Olefins. Carbonylation at a C-H Bond in the Benzene Ring", JOURNAL OF ORGANIC CHEMISTRY, (1997), vol. 62, no. 8, pages 2604 - 2610, XP002201286 [A] 1-11 * page 2606, column 2 *

DOI:   http://dx.doi.org/10.1021/jo970131r
 [A]  - GOSMINI C; NÉDÉLEC J Y; PÉRICHON J, "Electrosynthesis of functionalized 2-arylpyridines from functionalized aryl and pyridine halides catalyzed by nickel bromide 2,2'-bipyridine complex", TETRAHEDRON LETTERS, (2000), vol. 41, pages 5039 - 5042, XP002201287 [A] 1-11 * table 2 *

DOI:   http://dx.doi.org/10.1016/S0040-4039(00)00760-7
 [A]  - CACCHI S; FABRIZI G; MARINELLI F, "The Palladium-Catalyzed Transfer Hdrogenation/Heterocyclization of beta-(2-Aminophenyl)-alpha,beta-ynones. An Approach to 2-Aryl- and 2-Vinylquinolines", SYNLETT, (1999), XP002201288 [A] 1-11 * scheme 1, scheme 2, table 1, compound 1e *

DOI:   http://dx.doi.org/10.1055/s-1999-2629
 [A]  - BALDO M A ET AL, "VERY HIGH-EFFICIENCY GREEN ORGANIC LIGHT-EMITTING DEVICES BASED ON ELECTROPHOSPHORESCENCE", APPLIED PHYSICS LETTERS, AMERICAN INSTITUTE OF PHYSICS. NEW YORK, US, (19990705), vol. 75, no. 1, ISSN 0003-6951, pages 4 - 6, XP000850655 [A] 1-11 * the whole document *

DOI:   http://dx.doi.org/10.1063/1.124258
 [A]  - BALDO M A ET AL, "High-efficiency fluorescent organic light-emitting devices using a phosphorescent sensitizer", NATURE, MACMILLAN JOURNALS LTD. LONDON, GB, (20000217), vol. 403, no. 6771, ISSN 0028-0836, pages 750 - 753, XP002183466 [A] 1-11 * the whole document *

DOI:   http://dx.doi.org/10.1038/35001541
 [A]  - WANG, YUE ET AL, "(Hydroxyphenyl)pyridine derivative, its metal complexes and application a electroluminescence material", CAPLUS, CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US, Database accession no. 133:315395, URL: STN, XP002201289 [A] 1-11 * abstract *
 [A]  - DEDEIAN ET AL, "A NEW SYNTHETIC ROUTE TO THE PREPARATION OF A SERIES OF STRONG PHOTOREDUCING AGENTS: FAC TRIS-ORTHO-METALATED COMPLEXES OF IRIDIUM (III) WITH SUBSTITUTED 2-PHENYLPYRIDINES", INORGANIC CHEMISTRY, AMERICAN CHEMICAL SOCIETY, EASTON, US, (1991), vol. 30, no. 30, ISSN 0020-1669, pages 1685 - 1687, XP001070331 [A] 1-11 * the whole document *

DOI:   http://dx.doi.org/10.1021/ic00008a003
by applicantEP0443861
 US5247190
 US5408109
 US5552678
    - APPL. PHYS. LETT., (1999), vol. 75, page 4
    - POLYMER PREPRINTS, (2000), vol. 41, no. 1, page 770
    - O. LOHSE; P.THEVENIN; E. WALDVOGEL, SYNLETT, (1999), pages 45 - 48
    - MARKUS; JOHN, Electronics and Nucleonics Dictionary, MCGRAW-HILL, INC., (1966), page 470,476
    - "Flexible light-emitting diodes made from soluble conducting polymer", NATURE, (19920611), vol. 357, pages 477 - 479
    - Y. WANG, Kirk-Othmer Encyclopedia of Chemical Technology, (1996), vol. 18, pages 837 - 860
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.