Office Action Predictor
Last updated: April 15, 2026
Application No. 18/042,273

COMPOSITION FOR USE IN PHOTOELECTRONIC COMPONENT PACKAGING, PACKAGING STRUCTURE, AND PHOTOELECTRONIC COMPONENT

Non-Final OA §102
Filed
Feb 20, 2023
Examiner
MCCLENDON, SANZA L
Art Unit
1765
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Xi'An Smart Materials Co., LTD.
OA Round
1 (Non-Final)
81%
Grant Probability
Favorable
1-2
OA Rounds
2y 9m
To Grant
92%
With Interview

Examiner Intelligence

Grants 81% — above average
81%
Career Allow Rate
978 granted / 1213 resolved
+15.6% vs TC avg
Moderate +12% lift
Without
With
+11.7%
Interview Lift
resolved cases with interview
Typical timeline
2y 9m
Avg Prosecution
37 currently pending
Career history
1250
Total Applications
across all art units

Statute-Specific Performance

§101
0.2%
-39.8% vs TC avg
§103
38.0%
-2.0% vs TC avg
§102
32.5%
-7.5% vs TC avg
§112
17.2%
-22.8% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1213 resolved cases

Office Action

§102
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Claim Rejections - 35 USC § 102 The following is a quotation of the appropriate paragraphs of 35 U.S.C. 102 that form the basis for the rejections under this section made in this Office action: A person shall be entitled to a patent unless – (a)(1) the claimed invention was patented, described in a printed publication, or in public use, on sale, or otherwise available to the public before the effective filing date of the claimed invention. Claim(s) 1, 3, 8-9, 12-13 and 16 is/are rejected under 35 U.S.C. 102(a)(2) as being anticipated by Yu et al (CN102299118). Yu sets forth a method for packaging optoelectronic devices, wherein method comprises a thin-film packaging layer that is composed of an inorganic thin-film packaging material layer and an ultraviolet-sensitive material layer, which are alternately overlapped in layers from 1 to 20. Said ultraviolet-sensitive material comprises a 94-99.5 % of polythiol-polyene system; 0.2 to 1 % of a monofunctional or polyfunctional acrylic acid ester monomers; 0.1 to 5 % of a photoinitiator; 0.2 to 4 % of a photosensitizers and 0.2 to 4 % of additional additives, wherein the additives include antistatic agents, flame retardants, and coupling agents—see [0008]- [0013] and [0026]. Yu sets forth said coupling agents comprise compounds, such as methylvinyldichlorosilane, methylhydrodichlorosilane, dimethyldichlorosilane, dimethylmonochlorosilane, vinyltrichlorosilane, γ-aminopropyltrimethoxysilane, polydimethylsiloxane, polyhydromethylsiloxane, polymethylmethoxysilane, γ-propylmethacrylatetrimethoxysilane, γ-aminopropyltriethoxysilane, γ-glycidyl etherpropyltrimethoxysilane, aminopropylsilsesquioxane, γ-methacryloyloxypropyltrimethoxysilane, long-chain alkyltrimethoxysilane, vinyltriethoxysilane, vinyltrimethoxysilane, γ-chloropropyltriethoxysilane, bis-(γ-triethoxysilylpropyl), and anilinemethyltriethoxysilane. Silane, N-β(aminoethyl)-γ-aminopropyltrimethoxysilane, N-(β-aminoethyl)-γ-aminopropyltriethoxysilane, N-β(aminoethyl)-γ-aminopropylmethyldimethoxysilane, γ-(2,3-epoxypropoxy) propyltrimethoxysilane, γ-(methacryloyloxy) propyltrimethylsilane, γ-mercaptopropyltrimethoxysilane, γ-mercaptopropyltriethoxysilane—see [0075]. Yu sets forth said monofunctional or polyfunctional acrylic acid ester monomers include styrene, N-vinylpyrrolidone, isooctyl acrylate, hydroxyethyl acrylate and isobornyl acrylate, phosphate methacrylate and isobornyl methacrylate. Said polyfunctional monomers include triethylene glycol diacrylate, tripropylene glycol diacrylate, ethylene glycol diacrylate, polyethylene glycol (200) diacrylate, neopentyl glycol diacrylate, and propoxylated neopentyl glycol diacrylate, 1,6-hexanediol diacrylate (HDDA), 1,4-butanediol diacrylate (BDDA), propylene glycol diacrylate (DPGDA), glycerol diacrylate (TPGDA), and trifunctional trimethylolpropane triacrylate (TMPTA), pentaerythritol triacrylate (PETA), trimethylolpropane triacrylate (TMPTMA), trimethylolpropane triacrylate, propoxylated trimethylolpropane triacrylate, pentaerythritol tripropylene ester, propoxylated pentaerythritol propylene ester, N,N-dihydroxyethyl-3-aminopropionate methyl ester, and dimethylolpropane triacrylate. Ethylene glycol dimethacrylate, long-chain aliphatic hydrocarbon glycidyl ether acrylate, resorcinol diglycidyl ether, dipentaerythritol pentaacrylate, tripropylene glycol diacrylate, phthalic acid diethanol diacrylate (PDDA)—see [0053] to [0056]. Regarding claim 1: Yu sets forth by example a UV curable sealant composition comprising 55 parts of a UV curable organosiloxane obtained from the reaction product of a TDI trimer; dihydropolydiphenylsiloxane; hydroxyethyl acrylate; and 1,2-epoxy-4-hydroxylmethylcyclohexane; 10 parts of EHPE 3150 (multi-functional cycloaliphatic epoxy compound); 15 parts of Celloxide 2021P (3,4-Epoxycyclohexylmethyl-3′,4’epoxycyclohexanecarboxylate); 16 parts of MEDOL-10 (2-methyl-2-ethyl-1,3-dioxolane-4-yl)methyl acrylate); 2.2 parts of Irgacure 184 (a photoinitiator); 0.3 parts of Uyracure-160 (diphenyl[(phenylthio)phenyl]sulfonium hexafluorophosphate); and 1.5 parts by weight of methacryloxypropyl methoxydiethoxysilane—see example 1 in [0095]. It is deemed the 2-methyl-2-ethyl-1,3-dioxolane-4-yl) methyl acrylate (Medol-10) corresponds to applicants claimed photocurable monomer in claim 1 and the methacryloxypropylmethoxydiethoxysilane corresponds to the claimed monofunctional silane-containing monomer when R1 is a C1 (methyl) alkyl; X1 and X2 are C2 alkoxy (ethoxy) groups; n is 0; R2 is a C3 alkylene group; and R3 is a C1 (methyl) alkyl group. Regarding claims 3-4 and 13: Methacryloxypropylmethoxydiethoxysilane compound has a molecular weight of 260.40 g/mol and is represented by the formula: PNG media_image1.png 123 257 media_image1.png Greyscale , which corresponds to the third formula in claims 4 and 13. Regarding claims 8 and 16: Yu sets forth in the overall teachings photoinitiators, such as cleavage-type photoinitiators which include benzoin ethers (benzoin ethers), benzoin ketones, and acetophenones—see [0063]. Therefore, benzoin and acetophenone are anticipated. Additionally, photoinitiators such as acylphosphine oxides which include 2,4,6-trimethylbenzoyl diphenylphosphine oxide (TPO) and (2,4,6-trimethylbenzoyl) phenylphosphine oxide [BAPO phenyl bis(2,4,6-trimethylbenzoyl) phosphine oxide], phenyl bis(2,4,6-trimethylbenzoyl) phosphine oxide (819), tetramethylpiperidinone oxide (TMPO), and triethyl phosphate (TEPO) can also be used. Therefore, phosphorous photoinitiators are anticipated—see [0063]. Regarding claim 9: Yu sets forth in the overall teachings said optoelectronic devices are fabricated on clean, rigid substrates using high-vacuum evaporation, spin coating, self-assembly, inkjet printing, or screen printing and the UV curable material is cured by exposure to ultraviolet radiation—see [0020]. Regarding claim 12: Methacryloxypropylmethoxydiethoxysilane compound has a molecular weight of 260.40 g/mol. Allowable Subject Matter Claims 2, 5-7, 10-11, and 14-15 are objected to as being dependent upon a rejected base claim, but would be allowable if rewritten in independent form including all of the limitations of the base claim and any intervening claims. The following is a statement of reasons for the indication of allowable subject matter: The closest prior art Yu (cited above) fails to expressly teach and/or render obvious the tri-functional silicon-containing monomer represented by the formula found in claims 1-2, 11 and 13. Yu does not set forth the weight percentages as found in claims 5-7 and 14-15. Additionally, Yu does not expressly set forth the properties or structures set forth in claim 10. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to SANZA L MCCLENDON whose telephone number is (571)272-1074. The examiner can normally be reached 8-5. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Heidi Riviere-Kelley can be reached at 571-270-1831. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /SANZA L. McCLENDON/Primary Examiner, Art Unit 1765 SMc
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Prosecution Timeline

Feb 20, 2023
Application Filed
Nov 29, 2025
Non-Final Rejection — §102
Mar 23, 2026
Response Filed

Precedent Cases

Applications granted by this same examiner with similar technology

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A COMPOSITION FOR FAST-CURED THERMOSETS CONTAINING AMINES, THIOLS AND UNSATURATED MOLECULES
2y 5m to grant Granted Apr 14, 2026
Patent 12600820
PHOTOCURABLE COMPOSITION WITH HIGH SILICON CONTENT
2y 5m to grant Granted Apr 14, 2026
Patent 12590211
COMPOSITIONS AND METHODS OF MAKING A GREEN BODY OR A PRINTED ARTICLE USING THE SAME
2y 5m to grant Granted Mar 31, 2026
Patent 12583789
COMPOSITION FOR FORMING COATING LAYER OF OPTICAL FIBER AND CURED LAYER THEREOF, OPTICAL FIBER HAVING CURED LAYER, AND USE THEREOF
2y 5m to grant Granted Mar 24, 2026
Patent 12570782
FABRICATION OF SOLID MATERIALS OR FILMS FROM A POLYMERIZABLE LIQUID
2y 5m to grant Granted Mar 10, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

1-2
Expected OA Rounds
81%
Grant Probability
92%
With Interview (+11.7%)
2y 9m
Median Time to Grant
Low
PTA Risk
Based on 1213 resolved cases by this examiner. Grant probability derived from career allow rate.

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