JPH01500128A - ポリジアセチレン化合物を基礎とした温度指示薬 - Google Patents

ポリジアセチレン化合物を基礎とした温度指示薬

Info

Publication number: JPH01500128A
Authority: JP; Japan
Prior art keywords: polydiacetylene; compound; monomers; monomer; temperature indicator
Prior art date: 1986-04-30
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP62502794A

Other languages

English (en)

Japanese (ja)

Inventor

スイエリイ・アンネツテ

レ・モイネ・ジヤツクエス

Original Assignee

セントレ・ナシヨナル・デ・ラ・レチエルチエ・サイエンテイフイク

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1986-04-30

Filing date

1987-04-30

Publication date

1989-01-19

1987-04-30 Application filed by セントレ・ナシヨナル・デ・ラ・レチエルチエ・サイエンテイフイク filed Critical セントレ・ナシヨナル・デ・ラ・レチエルチエ・サイエンテイフイク

1989-01-19 Publication of JPH01500128A publication Critical patent/JPH01500128A/ja

Status Pending legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 title claims description 40
229920000015 polydiacetylene Polymers 0.000 title claims description 31
239000000178 monomer Substances 0.000 claims description 51
239000000203 mixture Substances 0.000 claims description 45
238000006116 polymerization reaction Methods 0.000 claims description 24
230000002427 irreversible effect Effects 0.000 claims description 9
-1 diacetylene compound Chemical class 0.000 claims description 8
238000010521 absorption reaction Methods 0.000 claims description 7
230000005855 radiation Effects 0.000 claims description 6
239000010409 thin film Substances 0.000 claims description 6
239000013078 crystal Substances 0.000 claims description 5
238000009281 ultraviolet germicidal irradiation Methods 0.000 claims description 5
239000010408 film Substances 0.000 claims description 4
239000000758 substrate Substances 0.000 claims description 3
229920001169 thermoplastic Polymers 0.000 claims description 2
239000004416 thermosoftening plastic Substances 0.000 claims description 2
229920000642 polymer Polymers 0.000 description 24
LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 description 21
230000007704 transition Effects 0.000 description 20
230000008859 change Effects 0.000 description 16
238000000034 method Methods 0.000 description 15
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
150000001345 alkine derivatives Chemical class 0.000 description 7
125000000217 alkyl group Chemical group 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 6
238000000862 absorption spectrum Methods 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 4
238000001816 cooling Methods 0.000 description 4
238000004817 gas chromatography Methods 0.000 description 4
JJGUXCMBZPRCDX-UHFFFAOYSA-N octadeca-7,9-diyne Chemical compound CCCCCCCCC#CC#CCCCCCC JJGUXCMBZPRCDX-UHFFFAOYSA-N 0.000 description 4
230000009257 reactivity Effects 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
101001018064 Homo sapiens Lysosomal-trafficking regulator Proteins 0.000 description 3
102100033472 Lysosomal-trafficking regulator Human genes 0.000 description 3
235000010703 Modiola caroliniana Nutrition 0.000 description 3
244000038561 Modiola caroliniana Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
239000002253 acid Substances 0.000 description 3
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Chemical class C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 3
238000004587 chromatography analysis Methods 0.000 description 3
230000021615 conjugation Effects 0.000 description 3
230000007423 decrease Effects 0.000 description 3
230000000694 effects Effects 0.000 description 3
125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 3
230000005496 eutectics Effects 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
239000002994 raw material Substances 0.000 description 3
230000002829 reductive effect Effects 0.000 description 3
239000000243 solution Substances 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
150000001879 copper Chemical class 0.000 description 2
OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
238000010586 diagram Methods 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
238000000605 extraction Methods 0.000 description 2
238000004949 mass spectrometry Methods 0.000 description 2
239000012528 membrane Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
238000010992 reflux Methods 0.000 description 2
230000002441 reversible effect Effects 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
238000000926 separation method Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
KOFZTCSTGIWCQG-UHFFFAOYSA-N 1-bromotetradecane Chemical compound CCCCCCCCCCCCCCBr KOFZTCSTGIWCQG-UHFFFAOYSA-N 0.000 description 1
WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical compound COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 description 1
125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
230000005526 G1 to G0 transition Effects 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
206010027476 Metastases Diseases 0.000 description 1
206010034972 Photosensitivity reaction Diseases 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
239000004411 aluminium Substances 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
238000009529 body temperature measurement Methods 0.000 description 1
238000007707 calorimetry Methods 0.000 description 1
150000001722 carbon compounds Chemical class 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
238000012412 chemical coupling Methods 0.000 description 1
238000000451 chemical ionisation Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000004581 coalescence Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000002131 composite material Substances 0.000 description 1
OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
238000007269 dehydrobromination reaction Methods 0.000 description 1
238000000113 differential scanning calorimetry Methods 0.000 description 1
208000002173 dizziness Diseases 0.000 description 1
JOOGVOJJNKEMAO-UHFFFAOYSA-N docosa-9,11-diyne Chemical compound CCCCCCCCCCC#CC#CCCCCCCCC JOOGVOJJNKEMAO-UHFFFAOYSA-N 0.000 description 1
KSOQHQONAHQOCM-UHFFFAOYSA-N dodeca-5,7-diyne Chemical compound CCCCC#CC#CCCCC KSOQHQONAHQOCM-UHFFFAOYSA-N 0.000 description 1
239000003814 drug Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
230000004907 flux Effects 0.000 description 1
235000013305 food Nutrition 0.000 description 1
230000004927 fusion Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000000769 gas chromatography-flame ionisation detection Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
PCTCNWZFDASPLA-UHFFFAOYSA-N hexa-2,4-diyne Chemical compound CC#CC#CC PCTCNWZFDASPLA-UHFFFAOYSA-N 0.000 description 1
NBHZWTSKGTYSSF-UHFFFAOYSA-N hexadeca-7,9-diyne Chemical compound CCCCCCC#CC#CCCCCCC NBHZWTSKGTYSSF-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000012535 impurity Substances 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
230000009401 metastasis Effects 0.000 description 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
238000000386 microscopy Methods 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
229910000069 nitrogen hydride Inorganic materials 0.000 description 1
LILZEAJBVQOINI-UHFFFAOYSA-N octa-3,5-diyne Chemical compound CCC#CC#CCC LILZEAJBVQOINI-UHFFFAOYSA-N 0.000 description 1
NKOICXZRKTWWME-UHFFFAOYSA-N octadeca-8,10-diyne Chemical compound CCCCCCCC#CC#CCCCCCCC NKOICXZRKTWWME-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000005691 oxidative coupling reaction Methods 0.000 description 1
239000000123 paper Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
230000036211 photosensitivity Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920001197 polyacetylene Chemical class 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000004237 preparative chromatography Methods 0.000 description 1
230000008569 process Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000033764 rhythmic process Effects 0.000 description 1
229910052594 sapphire Inorganic materials 0.000 description 1
239000010980 sapphire Substances 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000010183 spectrum analysis Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
239000004753 textile Substances 0.000 description 1
230000009466 transformation Effects 0.000 description 1
238000000411 transmission spectrum Methods 0.000 description 1
238000001429 visible spectrum Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F38/00—Homopolymers and copolymers of compounds having one or more carbon-to-carbon triple bonds
- G—PHYSICS
- G01—MEASURING; TESTING
- G01K—MEASURING TEMPERATURE; MEASURING QUANTITY OF HEAT; THERMALLY-SENSITIVE ELEMENTS NOT OTHERWISE PROVIDED FOR
- G01K11/00—Measuring temperature based upon physical or chemical changes not covered by groups G01K3/00, G01K5/00, G01K7/00 or G01K9/00
- G01K11/12—Measuring temperature based upon physical or chemical changes not covered by groups G01K3/00, G01K5/00, G01K7/00 or G01K9/00 using changes in colour, translucency or reflectance
- G01K11/16—Measuring temperature based upon physical or chemical changes not covered by groups G01K3/00, G01K5/00, G01K7/00 or G01K9/00 using changes in colour, translucency or reflectance of organic materials

Landscapes

Chemical & Material Sciences (AREA)
Physics & Mathematics (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Physics & Mathematics (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Measuring Temperature Or Quantity Of Heat (AREA)
Compositions Of Macromolecular Compounds (AREA)
Steroid Compounds (AREA)

JP62502794A 1986-04-30 1987-04-30 ポリジアセチレン化合物を基礎とした温度指示薬 Pending JPH01500128A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR8606320		1986-04-30
FR8606320A FR2598225B1 (fr)	1986-04-30	1986-04-30	Indicateurs de temperature a base de composes polydiacetyleniques

Publications (1)

Publication Number	Publication Date
JPH01500128A true JPH01500128A (ja)	1989-01-19

Family

ID=9334817

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP62502794A Pending JPH01500128A (ja)	1986-04-30	1987-04-30	ポリジアセチレン化合物を基礎とした温度指示薬

Country Status (9)

Country	Link
US (1)	US5085801A (de)
EP (1)	EP0248688B1 (de)
JP (1)	JPH01500128A (de)
AT (1)	ATE72328T1 (de)
DE (1)	DE3776409D1 (de)
ES (1)	ES2032300T3 (de)
FR (1)	FR2598225B1 (de)
GR (1)	GR3003913T3 (de)
WO (1)	WO1987006692A1 (de)

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JP2013512703A (ja) *	2009-12-02	2013-04-18	サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング	薬物送達デバイス及び関連包装

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US6861511B1 (en)	1986-06-04	2005-03-01	Bayer Corporation	Detection and quantification of neu related proteins in the biological fluids of humans
FR2656691A1 (fr) *	1990-01-03	1991-07-05	Dargent Yvon	Dispositif pour controler le respect d'une chaine du froid dans la distribution de produits a des temperatures negatives ou positives.
US5240643A (en) *	1992-03-11	1993-08-31	The United States Of America As Represented By The Secretary Of The Navy	Strain sensing composites
US5685641A (en) *	1996-01-16	1997-11-11	Ribi; Hans O.	Devices for rapid temperature detection
GB2310493B (en) *	1996-02-26	2000-08-02	Unilever Plc	Determination of the characteristics of fluid
US6043021A (en) *	1997-12-09	2000-03-28	Eastman Kodak Company	Packaged photographic product containing time and temperature integrating indicator device, and process for monitoring thermal exposure of photographic material
US6103351A (en) *	1997-12-09	2000-08-15	Eastman Kodak Company	Time and temperature integrating indicator device
US6113857A (en) *	1997-12-09	2000-09-05	Eastman Kodak Corporation	Gauge type time and temperature integrating indicator device
US5940637A (en) *	1997-12-09	1999-08-17	Eastman Kodak Company	Photographic film cartridge containing time and temperature integrating indicator device, and process for controlling photofinishing of film
CA2282084C (en)	1999-09-10	2005-01-11	Stuart A. Jackson	Radiation indicator device
US6610351B2 (en)	2000-04-12	2003-08-26	Quantag Systems, Inc.	Raman-active taggants and their recognition
US20030103905A1 (en) *	2000-06-23	2003-06-05	Ribi Hans O.	Methods and compositions for preparing consumables with optical shifting properties
US6607744B1 (en) *	2000-06-23	2003-08-19	Segan Industries	Ingestibles possessing intrinsic color change
US6787108B2 (en) *	2002-04-02	2004-09-07	Cmc Daymark Corporation	Plural intrinsic expiration initiation application indicators
US20050131355A1 (en) *	2002-06-12	2005-06-16	Fritz Kirchhofer	Injection or infusion device with refined surface
FR2864037B1 (fr) *	2003-12-22	2006-10-27	Tetra Laval Holdings & Finance	Systeme de bouchage avec controle d'effraction thermochrome
DE102006017579B3 (de) *	2006-04-13	2007-05-24	Infineon Technologies Ag	Ansteuerschaltung für ein Zündelement eines Sicherheitssystems
US7465693B2 (en) *	2006-09-13	2008-12-16	Flint Trading, Inc.	Thermochromatic temperature marking for outdoor surfaces
KR100930262B1 (ko) *	2007-08-13	2009-12-09	한국과학기술원	위조방지용지
WO2010009441A2 (en) *	2008-07-18	2010-01-21	Segan Industries, Inc.	Co-topo-polymeric compositions, devices and systems for controlling threshold and delay activation sensitivities
US20100029004A1 (en) *	2008-08-01	2010-02-04	Ribi Hans O	Duration and environmental monitoring compositions, devices methods for preparation and systems
US8569208B1 (en)	2008-12-23	2013-10-29	Segan Industries, Inc.	Tunable directional color transition compositions and methods of making and using the same
WO2011080529A1 (es) *	2009-12-29	2011-07-07	Aceites Y Grasas Vegetales S.A. Acegrasas S.A.	Producto oleoso indicador de freido
US8426856B2 (en)	2010-07-12	2013-04-23	International Business Machines Corporation	Thermally sensitive material embedded in the substrate
US9746380B2 (en)	2011-09-30	2017-08-29	Segan Industries, Inc.	Advanced multi-element consumable-disposable products
US20130098287A1 (en) *	2011-10-03	2013-04-25	Robert Parker	Microwave energy indicator
CN105283317B (zh)	2013-03-15	2018-02-06	西甘产业股份有限公司	用于在颜色变化组合物中降低背景色的化合物
GB201403391D0 (en) *	2014-02-26	2014-04-09	Protein Technologies Ltd	A method and device for monitoring substances
US20160194132A1 (en) *	2015-01-02	2016-07-07	Lara L. Davidson	Plastic-containing foodstuff containers using irreversible thermochromic material to indicate past exposure to elevated temperatures
CN113532683B (zh) *	2021-07-09	2022-06-03	江南大学	一种基于聚二乙炔脂质体的时间温度指示剂的制备方法
CN113755060B (zh) *	2021-09-16	2023-04-28	安徽师范大学	一种蓝相聚二乙炔复合材料及其制备方法和应用

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FR1525738A (fr) *	1966-06-06	1968-05-17	Battelle Development Corp	élément photosensible et procédé de formation d'image au moyen de cet élément
CA1043945A (en) *	1974-09-04	1978-12-05	Du Pont Of Canada Limited	Polymers of hydrocarbon-substituted diacetylene compounds
US3999946A (en) *	1976-02-23	1976-12-28	Allied Chemical Corporation	Time-temperature history indicators
US4215208A (en) *	1977-10-05	1980-07-29	Allied Chemical Corporation	Thermochromic polyacetylenes containing urethane groups
US4339951A (en) *	1977-10-05	1982-07-20	Allied Corporation	Tempeature measurement and display of indicia using thermochromic polyacetylenes
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US4195057A (en) *	1978-08-30	1980-03-25	Allied Chemical Corporation	Vapor-phase moving-boundary indicator
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DE3068767D1 (en) *	1980-03-27	1984-09-06	Allied Corp	Thermochromic polyacetylenic composition, process therefor, temperature measuring and indicia displaying devices and process for recording and thereafter erasing images
US4339240A (en) *	1980-05-07	1982-07-13	Allied Corporation	Color changing polyacetylenic compounds
US4624761A (en) *	1983-12-21	1986-11-25	Case Western Reserve University	Polymeric material composed of sheets of polydiacetylene and polyacetylene chains
US4788151A (en) *	1986-09-29	1988-11-29	Lifelines Technology, Inc.	Metal complexed acetylenic compounds useful as environmental indicating materials

1986
- 1986-04-30 FR FR8606320A patent/FR2598225B1/fr not_active Expired
1987
- 1987-04-30 ES ES198787401001T patent/ES2032300T3/es not_active Expired - Lifetime
- 1987-04-30 AT AT87401001T patent/ATE72328T1/de not_active IP Right Cessation
- 1987-04-30 EP EP87401001A patent/EP0248688B1/de not_active Expired - Lifetime
- 1987-04-30 JP JP62502794A patent/JPH01500128A/ja active Pending
- 1987-04-30 DE DE8787401001T patent/DE3776409D1/de not_active Expired - Lifetime
- 1987-04-30 WO PCT/FR1987/000145 patent/WO1987006692A1/fr not_active Ceased
1991
- 1991-06-19 US US07/717,869 patent/US5085801A/en not_active Expired - Fee Related
1992
- 1992-02-27 GR GR920400328T patent/GR3003913T3/el unknown

Cited By (1)

* Cited by examiner, † Cited by third party
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JP2013512703A (ja) *	2009-12-02	2013-04-18	サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング	薬物送達デバイス及び関連包装

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Publication number	Publication date
GR3003913T3 (de)	1993-03-16
EP0248688A1 (de)	1987-12-09
DE3776409D1 (de)	1992-03-12
ATE72328T1 (de)	1992-02-15
ES2032300T3 (es)	1993-02-01
US5085801A (en)	1992-02-04
FR2598225B1 (fr)	1988-08-26
EP0248688B1 (de)	1992-01-29
WO1987006692A1 (fr)	1987-11-05
FR2598225A1 (fr)	1987-11-06

Publication	Publication Date	Title
JPH01500128A (ja)	1989-01-19	ポリジアセチレン化合物を基礎とした温度指示薬
Cram et al.	1959	Macro Rings. XX. Transannular effects in π-π-Complexes1
Heesemann	1980	Studies on monolayers. 1. Surface tension and absorption spectroscopic measurements of monolayers of surface-active azo and stilbene dyes
US4189399A (en)	1980-02-19	Co-crystallized acetylenic compounds
US4384980A (en)	1983-05-24	Co-crystallized acetylenic compounds
Mapazi et al.	2017	A urea-modified polydiacetylene-based high temperature reversible thermochromic sensor: Characterisation and evaluation of properties as a function of temperature
US4235108A (en)	1980-11-25	Device for measuring temperature using co-crystallized acetylenic compositions
Pickett et al.	1936	The Ultraviolet Absorption Spectra of Substituted Biphenyls1
Malcolm	1966	Structural changes and molecular forces in a compressed synthetic polypeptide monolayer
Grummitt et al.	1951	Geometric Isomers of 1-Phenyl-1, 3-butadiene1
US4373032A (en)	1983-02-08	Metal salts of polyacetylenic compounds and uses thereof as ion exchange and thermochromic polymers
Gibson et al.	1981	Carbon-13 magic angle NMR study of the isomerization of cis-to trans-polyacetylene
Tieke et al.	1981	Topochemical reactions in Langmuir-Blodgett multilayers
TW200946649A (en)	2009-11-16	Polymerizable liquid crystal compound, polymerizable liquid crystal composition, liquid crystalline polymer, and optical isomer
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Sastry et al.	1999	Excess volumes, relative permittivity increments, and excess molar polarizations of {x CH2CCH3CO2CH3+ (1− x)(C6H6, or C7H8, or o-C8H10, or m-C8H10, or p-C8H10, or C8H10, or c-C6H12)}
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Moigne et al.	1989	Acetylenic and diacetylenic liquid-crystalline monomers: towards ordered conjugated polymers
Beaven et al.	1957	Steric Effects in the Gas–Liquid Chromatography of some Alkylbiphenyls
Worden Jr	1966	The effect of deuterium substitution on the intensity of the n→ π*(1U← 1A) absorption of some aliphatic carbonyl compounds
Fang	1986	HEPTACENE, OCTACENE, NONACENE, SUPERCENE, AND RELATED POLYMERS (POLYACENES, TWO-DIMENSIONAL POLYMERS, ACENEQUINONES, TETRAHALOHEPTIPTYCENE, BENT ANTHRACENE)
Lammertsma et al.	1979	1, 4, 5, 8-Tetramethylnaphthalene dication and related radical cations
Nakanishi et al.	1977	The crystal and molecular structure of dimethyl m-phenylenediacrylate.
Ando et al.	1971	Cyclic Acetylenes. XI. The Syntheses of p, p′-Bridged Cyclic Tolans by the Fritsch-Buttenberg-Wiechell Rearrangement

JPH01500128A - ポリジアセチレン化合物を基礎とした温度指示薬 - Google Patents

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