JPH0438336B2 - - Google Patents

Info

Publication number: JPH0438336B2
Authority: JP; Japan
Prior art keywords: deuterium; nonlinear optical; carbon; optical; heteroatom
Prior art date: 1986-07-16
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.): Expired

Application number

JP16553386A

Other languages

English (en)

Japanese (ja)

Other versions

JPS63163825A (ja

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.)

1986-07-16

Filing date

1986-07-16

Publication date

1992-06-24

1986-07-16 Application filed filed Critical

1986-07-16 Priority to JP16553386A priority Critical patent/JPS63163825A/ja

1988-07-07 Publication of JPS63163825A publication Critical patent/JPS63163825A/ja

1992-06-24 Publication of JPH0438336B2 publication Critical patent/JPH0438336B2/ja

Status Granted legal-status Critical Current

Links

230000003287 optical effect Effects 0.000 claims description 52
239000000463 material Substances 0.000 claims description 25
229910052799 carbon Inorganic materials 0.000 claims description 7
125000005842 heteroatom Chemical group 0.000 claims description 7
150000002894 organic compounds Chemical class 0.000 claims description 7
YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical group [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 6
229910052805 deuterium Inorganic materials 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
150000002431 hydrogen Chemical class 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
150000001412 amines Chemical class 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims description 3
239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 3
125000006575 electron-withdrawing group Chemical group 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims 1
150000005181 nitrobenzenes Chemical class 0.000 claims 1
WDCYWAQPCXBPJA-UHFFFAOYSA-N 1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1 WDCYWAQPCXBPJA-UHFFFAOYSA-N 0.000 description 19
238000000034 method Methods 0.000 description 11
230000000694 effects Effects 0.000 description 10
238000002485 combustion reaction Methods 0.000 description 5
239000013078 crystal Substances 0.000 description 5
230000006378 damage Effects 0.000 description 5
239000011368 organic material Substances 0.000 description 5
230000004044 response Effects 0.000 description 5
XTTIQGSLJBWVIV-UHFFFAOYSA-N 2-methyl-4-nitroaniline Chemical compound CC1=CC([N+]([O-])=O)=CC=C1N XTTIQGSLJBWVIV-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
230000005684 electric field Effects 0.000 description 4
229910010272 inorganic material Inorganic materials 0.000 description 4
239000011147 inorganic material Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
238000004891 communication Methods 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
230000010365 information processing Effects 0.000 description 3
230000007246 mechanism Effects 0.000 description 3
HSHNITRMYYLLCV-UHFFFAOYSA-N 4-methylumbelliferone Chemical compound C1=C(O)C=CC2=C1OC(=O)C=C2C HSHNITRMYYLLCV-UHFFFAOYSA-N 0.000 description 2
238000003763 carbonization Methods 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000005259 measurement Methods 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
230000015654 memory Effects 0.000 description 2
238000002156 mixing Methods 0.000 description 2
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
230000010355 oscillation Effects 0.000 description 2
230000010287 polarization Effects 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
230000008569 process Effects 0.000 description 2
238000012545 processing Methods 0.000 description 2
SXVAQZVQYFKMDP-UHFFFAOYSA-N 2-amino-2-(2,4-dinitrophenyl)butanoic acid Chemical compound CCC(N)(C(O)=O)C1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O SXVAQZVQYFKMDP-UHFFFAOYSA-N 0.000 description 1
SSOURMYKACOBIV-UHFFFAOYSA-N 3-methyl-4-nitro-1-oxidopyridin-1-ium Chemical class CC1=C[N+]([O-])=CC=C1[N+]([O-])=O SSOURMYKACOBIV-UHFFFAOYSA-N 0.000 description 1
ZETIVVHRRQLWFW-UHFFFAOYSA-N 3-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC(C=O)=C1 ZETIVVHRRQLWFW-UHFFFAOYSA-N 0.000 description 1
CJIJXIFQYOPWTF-UHFFFAOYSA-N 7-hydroxycoumarin Natural products O1C(=O)C=CC2=CC(O)=CC=C21 CJIJXIFQYOPWTF-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229910013641 LiNbO 3 Inorganic materials 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
230000008859 change Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000013461 design Methods 0.000 description 1
230000005686 electrostatic field Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
239000011521 glass Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
230000020169 heat generation Effects 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000000155 isotopic effect Effects 0.000 description 1
238000002372 labelling Methods 0.000 description 1
239000003446 ligand Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
GQYHUHYESMUTHG-UHFFFAOYSA-N lithium niobate Chemical compound [Li+].[O-][Nb](=O)=O GQYHUHYESMUTHG-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000012046 mixed solvent Substances 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000004570 mortar (masonry) Substances 0.000 description 1
238000006396 nitration reaction Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
230000009022 nonlinear effect Effects 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
230000008832 photodamage Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000012827 research and development Methods 0.000 description 1
229910052711 selenium Inorganic materials 0.000 description 1
238000000935 solvent evaporation Methods 0.000 description 1
125000006850 spacer group Chemical group 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229910052714 tellurium Inorganic materials 0.000 description 1
238000010998 test method Methods 0.000 description 1
230000007704 transition Effects 0.000 description 1
ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 description 1
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
235000012141 vanillin Nutrition 0.000 description 1
238000011179 visual inspection Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/35—Non-linear optics
- G02F1/355—Non-linear optics characterised by the materials used
- G02F1/361—Organic materials

Landscapes

Physics & Mathematics (AREA)
Nonlinear Science (AREA)
General Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP16553386A 1986-07-16 1986-07-16 重水素置換有機非線形光学材料 Granted JPS63163825A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP16553386A JPS63163825A (ja)	1986-07-16	1986-07-16	重水素置換有機非線形光学材料

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP16553386A JPS63163825A (ja)	1986-07-16	1986-07-16	重水素置換有機非線形光学材料

Publications (2)

Publication Number	Publication Date
JPS63163825A JPS63163825A (ja)	1988-07-07
JPH0438336B2 true JPH0438336B2 (de)	1992-06-24

Family

ID=15814198

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP16553386A Granted JPS63163825A (ja)	1986-07-16	1986-07-16	重水素置換有機非線形光学材料

Country Status (1)

Country	Link
JP (1)	JPS63163825A (de)

1986
- 1986-07-16 JP JP16553386A patent/JPS63163825A/ja active Granted

Also Published As

Publication number	Publication date
JPS63163825A (ja)	1988-07-07

Publication	Publication Date	Title
US5670091A (en)	1997-09-23	Nonlinear optical materials with reduced aromaticity and bond length alternation
Shettigar et al.	2008	Studies on third-order nonlinear optical properties of chalcone derivatives in polymer host
DE4234230C2 (de)	2003-08-14	Substituierte Thieno[3,2-b]thiophene und ihre Verwendung
Naseema et al.	2010	Synthesis, characterization and studies on the nonlinear optical parameters of hydrazones
US4707303A (en)	1987-11-17	High performance nonlinear optical substrates
Ray et al.	1995	First-order hyperpolarizabilities of sulfophthalein dyes
Duan et al.	1995	Second-order hyperpolarizabilities of organic ionic species
Soileau et al.	1985	Studies of the nonlinear switching properties of liquid crystals with picosecond pulses
JPH0438336B2 (de)	1992-06-24
JPH0438335B2 (de)	1992-06-24
Takeda et al.	1998	Intramolecular proton transfer of a 2-(2′, 4′-dinitrobenzyl) pyridine studied by femtosecond transient absorption spectroscopy
US4966730A (en)	1990-10-30	Nonlinear optical devices from derivatives of stilbene and diphenylacetylene
JP2783869B2 (ja)	1998-08-06	非線形光学素子
DE19537969A1 (de)	1997-04-17	Verwendung von Spiroverbindungen als Werkstoffe in der nicht-linearen Optik
JPS63261233A (ja)	1988-10-27	２次の非線形光学材料
US4909608A (en)	1990-03-20	Optical monlinearity of aminobenzophenone derivatives
JP2694562B2 (ja)	1997-12-24	新規な有機非線形光学材料およびそれを用いた光波長の変換方法
JP2539834B2 (ja)	1996-10-02	非線形光学素子
JPH06118462A (ja)	1994-04-28	有機非線形光学材料
JPH04277724A (ja)	1992-10-02	有機非線形光学材料
JPH01185527A (ja)	1989-07-25	非線形光学材料
Xu et al.	2025	New thioxanthene-Phenothiazine derivatives: synthesis, characterization and third-order nonlinear optical (NLO) properties
JP2539840B2 (ja)	1996-10-02	非線形光学素子
Shettigar et al.	2007	Effect of polymer host on third order nonlinear optical properties of newly synthesized organic liquid crystal
JPH04319922A (ja)	1992-11-10	有機非線形光学材料