Ex Parte HUNG et alDownload PDFPatent Trial and Appeal BoardJul 31, 201713569397 (P.T.A.B. Jul. 31, 2017) Copy Citation United States Patent and Trademark Office UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O.Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 13/569,397 08/08/2012 Gavin HUNG MERCK-3981 9138 23599 7590 08/02/2017 MILLEN, WHITE, ZELANO & BRANIGAN, P.C. 2200 CLARENDON BLVD. SUITE 1400 ARLINGTON, VA 22201 EXAMINER MALLOY, ANNA E ART UNIT PAPER NUMBER 1722 NOTIFICATION DATE DELIVERY MODE 08/02/2017 ELECTRONIC Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address(es): docketing@mwzb.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte GAVIN HUNG, ROGER CHANG, KRIS TSAI, and GLAVIN OYANG Appeal 2016-005218 Application 13/569,397 Technology Center 1700 Before CHRISTOPHER L. CRUMBLEY, JULIA HEANEY, and MICHAEL G. McMANUS, Administrative Patent Judges. McMANUS, Administrative Patent Judge. DECISION ON APPEAL The Examiner finally rejected claims 1—5, 7—18, and 20-23 of Application 13/569,397 under 35 U.S.C. § 103(a) as obvious. Final Act. 2—13 (June 12, 2014). Appellants1 seek reversal of these rejections pursuant to 35 U.S.C. § 134(a). We have jurisdiction under 35 U.S.C. § 6. For the reasons set forth below, we AFFIRM. 1 MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG is identified as the real party in interest. Appeal Br. 1. Appeal 2016-005218 Application 13/569,397 BACKGROUND The present application generally relates to liquid-crystalline media and the use of such media in electro-optical liquid-crystal displays. Abst. Claims 1 and 23 are representative of the pending claims and are reproduced below: 1. Liquid-crystalline medium, comprising: - a polymerisable component (A) comprising one or more polymerisable compounds and - a liquid crystalline component (B) containing one or more compounds of the general formula I and one or more compounds of the general formula IA wherein R° denotes an alkyl or alkoxy radical having 1 to 15 C atoms, where, in addition, one or more CH2 groups in these radicals may each be replaced, independently of one another, by -C=C-, -CF20-, - CHCH-, -O' ? -00-, -0-, -CO-O, or-O-CO- 2 Appeal 2016-005218 Application 13/569,397 in such a way that O atoms are not linked directly to one another, and where, in addition, one or more H atoms may be replaced by halogen atoms, X° denotes F, Cl, CN, SF5, SCN, NCS, a halogenated alkyl radical, a halogenated alkenyl radical, a halogenated alkoxy radical or a halogenated alkenyloxy radical having up to 6 C atoms, and L1'6 each, independently of one another, denote H or F. 23. The liquid-crystalline medium of claim 2, wherein P1 and P2 each, independently of one another, denote, an acrylate, methacrylate, fluoroacrylate, oxetane, vinyl, vinyloxy or epoxide group, Sp1 and Sp2 denote -(CH2)pi-, -(CH2)pi-0-, -(CH2)pi-CO- O- or -(CH2)pi-0-C0-0-, wherein pi is an integer from 1 to 12, and where the linking to the adjacent ring in the last-mentioned groups takes place via the O atom, Raa denotes straight-chain or branched, optionally mono- or polyfluorinated alkyl, alkoxy, alkenyl, alkynyl, alkylcarbonyl, alkoxycarbonyl, alkylcarbonyloxy or alkoxycarbonyloxy having 1 to 12 C atoms where the alkenyl and alkynyl radicals have at least two C atoms and the branched radicals have at least three C atoms, and L is fluorine. Claims Appendix 2—3, 31—32 (Sept. 10, 2015). 3 Appeal 2016-005218 Application 13/569,397 REJECTIONS On appeal, the Examiner maintains the following rejections:2 1. Claims 1—4, 7—18, and 20—22 are rejected under 35 U.S.C. § 103(a) as obvious over Wittek et al. (WO 2011/076329 Al, pub. June 30, 2011) (hereinafter “Wittek”).3 Final Act. 3—8. 2. Claims 1, 4, 5, 7—16, 18, and 20—22 are rejected under 35 U.S.C. § 103(a) as obvious over Fujita (US 2011/0127465 Al, pub. June 2, 2011). Id. at 8-11. 3. Claim 23 is rejected under 35 U.S.C. § 103(a) as obvious over Wittek in view of Goetz et al. (WO 2011/050893 Al, pub. May 5, 2011) (hereinafter “Goetz”).4 Id. at 11—12. 4. Claims 2, 3, 17, and 23 are rejected under 35 U.S.C. § 103(a) as obvious over Fujita in view of Goetz. Id. at 12—13. DISCUSSION Rejection 1. The Examiner rejected claims 1—4, 7—18, and 20-22 as obvious over Wittek. Id. at 3—8. Wittek’s disclosure indicates that the inventive medium “comprises one or more compounds of the formula I” followed by a description of such formula. Wittek 126. Wittek then teaches that the medium “additionally 2 In the Final Rejection, the Examiner rejected claims 4 and 8 as indefinite. Final Act. 2—3. This rejection was subsequently withdrawn in view of an amendment to the claims. Answer 2. 3 The Examiner relies upon United States counterpart application US 2012/0273723 Al, pub. Nov. 1, 2012, as an English translation of Wittek. 4 The Examiner relies upon United States counterpart application US 2012/0224124 Al, pub. Sept. 6, 2012, as an English translation of Goetz. 4 Appeal 2016-005218 Application 13/569,397 comprises one or more neutral compounds of the formulae II and/or III.” Id. | 58. Wittek’s disclosure continues in a similar manner through formula XXVII with certain formulae grouped together (e.g. “one or more tetracyclic compounds selected from the formulae XIX to XXVII”). Id. 59—129. Wittek’s specification further lists certain compounds of the various formulae in Tables A and B and states that “[preferred mixture components are shown in Tables A and B.” Id. 1179. Wittek additionally includes examples of specific liquid-crystalline media. One such example is Example Ml. Id. 1197. Example Ml describes a medium that includes compounds APUQU-2-F and DPGU-4-F. Id. The Examiner finds that compound DPGU-4-F falls within formula I of claim 1. Answer 20. The Examiner further finds that compound APUQ-2-F is listed in Wittek’s specification as a compound of formula XI. Id. (citing Wittek 1103). Wittek teaches that the inventive medium comprises “one or more compounds selected from the following formulae” followed by formulae X and XI. Id. 1101. It then lists several compounds including APUQU-n-F and Xe. Compound Xe corresponds to formula IA of claim 1. In view of the teaching to include one or more of the compounds of formulae X and XI, the Examiner concludes that the compounds are equivalent. Answer 20—24. The Examiner further relies on the teaching of Wittek that, in order to set the desired tilt angle, polymerizable compounds can be added to the medium. Id. at 20 (citing Wittek 1177, Table E). Appellants do not dispute that Wittek teaches compounds of formulae I and IA (of the claims) as well as polymerizable compounds. Appeal Br. 3; Reply 9. Rather, Appellants argue that the rejection is erroneous because Wittek teaches a large number of compounds and provides no teaching that “the particular compounds of the claims should be selected and combined.” 5 Appeal 2016-005218 Application 13/569,397 Appeal Br. 4. Appellants further argue that the Examiner improperly relies upon Example Ml of Wittek. Id. at 5—6. Appellants assert that “[o]ne skilled in the art would clearly not read example Ml as inviting additional components and would have no reason to select the [sic] specifically the Xe compound from the hundreds of thousands of other possible compounds to choose from in Wittek.” Id. at 6. Wittek’s inclusion of a number of compounds as possible components of the liquid-crystalline medium does not make the selection of any particular compound less obvious. “That the [prior art reference] discloses a multitude of effective combinations does not render any particular formulation less obvious. This is especially true because the claimed composition is used for the identical purpose taught by the prior art.” Merck & Co. v. Biocraft Labs., Inc., 874 F.2d 804, 807 (Fed. Cir. 1989); see also In re Susi, 440 F.2d 442, 445 (1971) (obviousness rejection affirmed where the disclosure of the prior art was “huge, but it undeniably include [d] at least some of the compounds recited in appellant’s generic claims and it is of a class of chemicals to be used for the same purpose as appellant’s additives”). Nor have Appellants shown error in the Examiner’s finding that a person of ordinary skill in the art would know that one may substitute compound Xe for compound APUQU-2-F. Wittek’s teaching to use “one or more compounds” of formulae X and XI, treated collectively, suggests an equivalent function. Accordingly, one of skill in the art would know that one could substitute one such compound for another in a liquid-crystalline composition. In view of the foregoing, Appellants have not shown error in the Examiner’s finding of obviousness of claims 1—4, 7—18, and 20-22. 6 Appeal 2016-005218 Application 13/569,397 Rejection 2. The Examiner rejected claims 1, 4, 5, 7—16, 18, and 20—22 as obvious over Fujita. Final Act. 8—11. The rejection of these claims over Fujita is similar to Rejection 1 over Wittek. In the present rejection, the Examiner looks to Fujita’s Example 4 which teaches to include compound 3-HGB(F,F)XB(F,F)-F, which the Examiner finds is equivalent to formula IA of claim 1, and several compounds of Fujita’s formula 6. Answer 13. Fujita depicts formula 6 as follows: Fujita 125. Fujita teaches that ring C may independently include 3,5-difhioro-l,4-phenylene and/or l,3-dioxane-2,5-diyl. Id. Fujita further teaches that Z1 may be a single bond. Id. Accordingly, embodiments of formula 6 fall within the scope of formula I of the present claim 1. As a specific example, the Examiner cites to compound 6-13 as a particular compound of Fujita’s formula 6 falling within the scope of formula 1 of claim 1. Answer 13; Fujita 1 56. Additionally, Fujita teaches to incorporate at least one compound of formula 6 in the FC medium composition. Fujita teaches an embodiment (referred to as an “item”) comprising the “composition according to any one of items 1 to 9, further including at least one compound selected from the group of compounds represented by formula (6) as a sixth component.” Id. 125. 7 Appeal 2016-005218 Application 13/569,397 The Examiner finds that a person of ordinary skill in the art would regard the several compounds of formula 6 listed in Example 4 (variants of compounds 6-4 and 6-5) as equivalent to compound 6-13. Asa consequence, the Examiner finds, it would have been obvious to one of ordinary skill in the art at the time the invention was made to either add an additional compound of formula 6 (such as compound 6-13) to the exemplary composition or to substitute compound 6-13 for one of the other listed compounds of Fujita’s formula 6. Answer 13. The Examiner additionally finds that Fujita teaches to add polymerizable compounds. Answer 16 (citing Fujita 58, 63). In this regard, Fujita discloses that “additives which may be mixed with the composition will be explained. The additives include ... a polymerizable compound and a polymerization initiator.” Fujita 1 58. Fujita additionally teaches that a “polymerizable compound is mixed with the composition for adjusting to a device having a polymer sustained alignment (PSA) mode.” Id. 163. Appellants argue that “the mere existence of these two compounds amongst the many thousands of other compounds generically encompassed by Fujita fails to provide any reason for one skilled in the art to select these two compounds and combine them.” Appeal Br. 6; see also Reply 1—2. Appellants also argue that “Fujita teaches the examples, including Example 4, as closed.” Reply 2. As above, a prior art reference’s inclusion of a “multitude” of compounds as possible components of a composition does not limit the scope of the disclosure. Merck & Co. v. Biocraft Labs., Inc., 874 F.2d at 807. Moreover, Appellants have not shown error in the Examiner’s stated reason why a person of ordinary skill in the art would know that Example 4 8 Appeal 2016-005218 Application 13/569,397 could be modified. Fujita teaches an embodiment “further including at least one compound selected from the group of compounds represented by formula (6) as a sixth component.” Fujita 125. Fujita further teaches that “[t]he sixth component is desirable for the preparation of a composition having a large dielectric anisotropy.” Id. |44. Appellants have not shown error in the Examiner’s finding of equivalent function among the compounds of formula 6. Accordingly, Appellants have not shown error in the Examiner’s finding of obviousness of claims 1, 4, 5, 7—16, 18, and 20-22. Rejection 3. The Examiner rejected claim 23 as obvious over Wittek in view of Goetz. Final Act. 11—12. The Examiner found that Goetz teaches certain claimed polymerizable compounds. Id. at 12. Appellants argue that a person of ordinary skill in the art would not combine the teachings of Wittek and Goetz because Goetz is directed to the use of polymerizable compounds in liquid crystalline mixtures having a negative dielectric anisotropy while Wittek is directed to liquid crystalline mixtures having a positive dielectric anisotropy. Appeal Br. 8. Appellants assert that one of ordinary skill in the art “would understand that the mixture concepts of negative LC mixtures and positive LC mixtures are different and teaching[s] are not transferable between the two.” Id. The Examiner, however, points out that Goetz teaches an embodiment where “the LC medium comprises an LC host mixture based on compounds having positive dielectric anisotropy.” Answer 25 (citing Goetz 1200) (emphasis added). The Examiner finds that Wittek teaches electro-optical displays such as TN, IPS, and FFS and that Goetz teaches that polymerizable compounds can be added to both positive and negative liquid crystal 9 Appeal 2016-005218 Application 13/569,397 compositions for use in TN, IPS, and FFS displays. Id. at 25—26 (citing Goetz 1200 and Wittek 1162). In view of the foregoing, Appellants have failed to show error in the Examiner’s reason to combine the teachings of Wittek and Goetz. Rejection 4. The Examiner rejected 2, 3, 17, and 23 as obvious over Fujita in view of Goetz. Final Act. 12—13. Appellants argue that the Examiner has failed to state a basis why one skilled in the art would combine the teachings of these two references Appeal Br. 9. In drafting Rejection 4, the Examiner indicated that the rejection is predicated upon Fujita and Goetz. Final Act. 12. In stating the reason to combine the teachings of Fujita and Goetz, however, the Examiner stated that “it would have been obvious to one of ordinary skill in the art at the time the invention was made to use the polymerizable compound RM-29 of Goetz et al. as the polymerizable compound of Wittek since Goetz teaches polymerizable compound RM-1 and RM-29 are equivalent.” Id. at 13 (emphasis added). That is, the Examiner referred to Wittek rather than Fujita. On this basis, Appellants argue that “the Examiner provides no reason why one skilled in the art would combine the two.” Appeal Br. 9. Appellants, however, acknowledge that “[t]he Examiner appears to have made a copy and paste error or confused which references were included in the rejection.” This understanding is confirmed by the Examiner. Answer 18 (“The Examiner apologizes for the copy and paste error recited in the Final Office Action. It should read Fujita and not Wittek.”). Appellants did not seek to have the foregoing designated as a new ground of rejection. Accordingly, any such argument is waived. 37 CFR§ 41.40(a). 10 Appeal 2016-005218 Application 13/569,397 In view of the foregoing, and the record as a whole, we find that Appellants have not shown that the Examiner failed to state a reason to combine the teachings of Fujita and Goetz. Appellants additionally argue that a person of ordinary skill in the art would not combine the teachings of Fujita and Goetz for the same reason as posited with regard to Rejection 3 — that Goetz teaches adding polymerizable compounds only to compositions with negative dielectric anisotropy. Appeal Br. 9. For the reasons stated in regard to Rejection 3 we determine that Goetz also teaches an embodiment where “the FC medium comprises an FC host mixture based on compounds having positive dielectric anisotropy.” Goetz 1200; see also Wittek 1162. CONCFUSION The rejection of claims 1—4, 7—18, and 20-22 as obvious over Wittek is affirmed. The rejection of claims 1, 4, 5, 7—16, 18, and 20—22 as obvious over Fujita is affirmed. The rejection of claim 23 as obvious over Wittek in view of Goetz is affirmed. The rejection of claims 2, 3, 17, and 23 over Fujita in view of Goetz is affirmed. No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a). AFFIRMED 11 Copy with citationCopy as parenthetical citation