Latent imaging for volume Bragg gratings

US11634528B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11634528-B2
Application numberUS-202016865022-A
CountryUS
Kind codeB2
Filing dateMay 1, 2020
Priority dateMay 8, 2019
Publication dateApr 25, 2023
Grant dateApr 25, 2023

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Initiator/mediator chemistry for latent imaging polymers for volume Bragg gratings is provided. Light mediated chemistry including the use of nitroxides allows a first step imaging to occur, where a light induced pattern is recorded in the material, without the grating being apparent. A second bleaching/developing step completes the curing process and reveals the grating.

First claim

Opening claim text (preview).

The invention claimed is: 1. A polymeric material comprising a resin mixture comprising: a partially or completely polymerized or crosslinked polymer matrix; a polymer precursor comprising a monomer M; and a group of Formula I: wherein IN is an initiating moiety optionally linked to, or part of, the matrix, -[M]- is a polymerized monomer, x is an integer from 0 to 50, and the group of Formula I is anisotropically distributed throughout the polymeric material. 2. The polymeric material of claim 1 , wherein IN is linked to, or part of, the matrix, as in Formula II: 3. The polymeric material of claim 1 , wherein IN comprises an alkyl amine or a carboxyl group. 4. The polymeric material of claim 1 , wherein x is 0, as in Formula III: and wherein is an optional link to the matrix. 5. The polymeric material of claim 2 , wherein the group of Formula II is selected from the groups of Formulas 101 to 106, wherein is an optional link to the matrix: 6. The polymeric material of claim 1 , wherein M is selected from an optionally substituted acrylate, an optionally substituted methacrylate, an optionally substituted acrylamide, an optionally substituted methacrylamide, an optionally substituted styrene, an optionally substituted vinyl derivative, and an optionally substituted allyl derivative. 7. The polymeric material of claim 1 , wherein x is at least 1, and -[M]- is selected from a polymerized optionally substituted acrylate, a polymerized optionally substituted methacrylate, a polymerized optionally substituted acrylamide, a polymerized optionally substituted methacrylamide, a polymerized optionally substituted styrene, a polymerized optionally substituted vinyl derivative, and a polymerized optionally substituted allyl derivative. 8. The polymeric material of claim 2 , wherein Formula II is selected from the groups of Formulas 1001 to 1011: wherein: x is at least 1; R 1 is selected from hydrogen, optionally substituted alkyl, optionally substituted heteroalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, and optionally substituted heteroarylalkyl; R 2 is independently a group of one, two, three, or four independently selected substituents, or no substituent, each substituent independently comprising one or more groups selected from optionally substituted alkyl, optionally substituted heteroalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, hydroxy, halo, cyano, trifluoromethyl, trifluoromethoxy, nitro, trimethylsilanyl, —OR a , —SR a , —OC(O)—R a , —N(R a ) 2 , —C(O)R a , —C(O)OR a , —OC(O)OR a , —OC(O)N(R a ) 2 , —C(O)N(R a ) 2 , —N(R a )C(O)OR a , —N(R a )C(O)R a , —N(R a )C(O)N(R a ) 2 , N(R a )C(NR a )N(R a ) 2 , —N(R a )S(O) t R a (where t is 1 or 2), —S(O) t OR a , —S(O) t N(R a ) 2 , —S(O) t N(R a )C(O)R a , (O)P(OR a ) 3 , (S)P(OR a ) 3 , and —(O)P(OR a ) 2 ; R 3 is selected from optionally substituted alkyl, optionally substituted heteroalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, trifluoromethyl, trifluoromethoxy, nitro, trimethylsilanyl, —OR a , —SR a , —OC(O)—R a , —N(R a ) 2 , —C(O)R a , —C(O)OR a , —OC(O)OR a , —OC(O)N(R a ) 2 , —C(O)N(R a ) 2 , —N(R a )C(O)OR a , —N(R a )C(O)R a , —N(R a )C(O)N(R a ) 2 , N(R a )C(NR a )N(R a ) 2 , —N(R a )S(O) t R a , —S(O) t OR a , —S(O) t N(R a ) 2 , —S(O) t N(R a )C(O)R a , —O(O)P(OR a ) 2 , and —O(S)P(OR a ) 2 ; t is 1 or 2; and R a is independently selected from hydrogen, optionally substituted alkyl, optionally substituted heteroalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, and optionally substituted heteroarylalkyl. 9. The polymeric material of claim 1 , wherein the polymer matrix comprises a polyurethane fragment. 10. The polymeric material of claim 1 , wherein portions of material having a higher concentration of Formula I form a virtual Bragg grating, wherein the grating is characterized by a Q parameter equal to or greater than 5, wherein Q = 2 ⁢ πλ 0 ⁢ d n 0 ⁢ Λ 2 and wherein λ 0 is a recording wavelength, d is the thickness of the recording material, n 0 is a refractive index of the recording material, and Λ is a grating constant.

Assignees

Inventors

Classifications

  • Manufacturing methods · CPC title

  • for storing optical interference patterns, e.g. holograms; for storing data in three dimensions [3D], e.g. volume storage (G11B7/24038 takes precedence) · CPC title

  • Stable Free Radical Polymerisation [SFRP]; Nitroxide Mediated Polymerisation [NMP] for, e.g. using 2,2,6,6-tetramethylpiperidine-1-oxyl [TEMPO] · CPC title

  • Holograms used as optical elements · CPC title

  • having holographic or diffractive elements (diffraction gratings per se G02B5/18; holographic elements per se G02B5/32; generating the spectrum using diffraction elements G01J3/18) · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11634528B2 cover?
Initiator/mediator chemistry for latent imaging polymers for volume Bragg gratings is provided. Light mediated chemistry including the use of nitroxides allows a first step imaging to occur, where a light induced pattern is recorded in the material, without the grating being apparent. A second bleaching/developing step completes the curing process and reveals the grating.
Who is the assignee on this patent?
Meta Platforms Tech Llc
What technology area does this patent fall under?
Primary CPC classification C08F283/006. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 25 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).