Production Method 1

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran

Reference

Multi-stimuli responsive fluorescence of amphiphilic AIEgen copolymers for ultrafast, highly sensitive and selective copper ion detection in water

Nhien, Pham Quoc ; Wu, Po-Hsun; Wu, Chia-Hua; Wu, Judy I.; Hue, Bui Thi Buu; et al, Sensors and Actuators, 2021, 344,

Production Method 2

68161-05-7

919789-77-8

Reaction Conditions

1.1 Reagents: Boron tribromide Solvents: Dichloromethane ;  0 °C; 24 h, 0 °C → rt
1.2 Reagents: Water

Reference

Proton conducting hybrid membrane electrolytes of sulfonated poly(ether sulfone)s and poly(ether sulfone)s containing metallophthalocyanine

Lim, Youngdon; Lee, Soonho; Seo, Dongwan; Jang, Hohyoun; Hossain, Awlad Md; et al, International Journal of Hydrogen Energy, 2014, 39(3), 1539-1548

Production Method 3

68161-05-7

919789-77-8

Reaction Conditions

1.1 Reagents: Boron tribromide Solvents: Dichloromethane ;  1 h, -45 °C; 6 h, rt

Reference

Thiophenol detection using an AIE fluorescent probe through self-assembly with TPE-based glycoclusters

Dong, Lei; Chen, Guo-Rong; He, Xiao-Peng; Vidal, Sebastien, Organic & Biomolecular Chemistry, 2019, 17(41), 9251-9256

Production Method 4

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Catalysts: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  -78 °C; 30 min, -78 °C; 8 h, -78 °C → rt; 15 h, 70 °C; cooled
1.2 Reagents: Potassium carbonate Solvents: Water

Reference

Electrochromic/electrofluorochromic poly(urea-urethane) bearing oligoaniline and tetraphenylethylene groups: Synthesis, characterization, and H2O2 visualized determination

Zhang, Yingchao; Xie, Yunfei; Zhou, Mingjuan; Berda, Erik B.; Chao, Danming, Dyes and Pigments, 2021, 194,

Production Method 5

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  rt → -5 °C; 10 °C; 10 °C → rt; 0.5 h, rt; 2.5 h, reflux; reflux → -5 °C
1.2 Reagents: Piperidine ;  10 min, -5 - 0 °C
1.3 Solvents: Tetrahydrofuran ;  -5 - 0 °C; -5 °C → reflux; 20 - 30 h, reflux
1.4 Reagents: Potassium carbonate Solvents: Water

Reference

A facile synthesis of tetraarylethenes via cross McMurry coupling between diaryl ketones

Duan, Xin-Fang; Zeng, Jing; Lu, Jia-Wei; Zhang, Zhan-Bin, Synthesis, 2007, (5), 713-718

Production Method 6

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  0 °C; 2 h, 0 °C → reflux
1.2 Solvents: Tetrahydrofuran ;  reflux; overnight, reflux
1.3 Reagents: Sodium bicarbonate Solvents: Water ;  pH 7

Reference

Cationic fluorescent probe based on tetraphenyl ethylene structure

, China, , ,

Production Method 7

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc Catalysts: Titanium tetrachloride Solvents: Tetrahydrofuran ;  cooled; rt; overnight, reflux
1.2 Reagents: Potassium carbonate Solvents: Water ;  30 min, reflux

Reference

Porous Organic Polymer from Aggregation-Induced Emission Macrocycle for White-Light Emission

Wang, Zhen; Yan, Sen; Cui, Huang-Chen; Cheng, Guang; Ma, Hui; et al, Macromolecules (Washington, 2018, 51(19), 7863-7871

Production Method 8

68161-05-7

919789-77-8

Reaction Conditions

1.1 Reagents: Boron tribromide Solvents: Dichloromethane ;  1 h, 0 °C; overnight, rt
1.2 Reagents: Sodium bicarbonate Solvents: Water ;  cooled

Reference

Bimodal Fluorescence-Magnetic Resonance Contrast Agent for Apoptosis Imaging

Li, Hao; Parigi, Giacomo ; Luchinat, Claudio; Meade, Thomas J., Journal of the American Chemical Society, 2019, 141(15), 6224-6233

Production Method 9

68161-05-7

919789-77-8

Reaction Conditions

1.1 Reagents: Boron tribromide Solvents: Dichloromethane ;  -78 °C; 1 h, -78 °C; -78 °C → rt; 12 h, rt
1.2 Reagents: Water ;  cooled

Reference

Process for preparation of zwitterion-modified tetraphenylethylene and application as cathode interfacial modification material bulk-heterojunction polymer solar cell

, China, , ,

Production Method 10

68161-05-7

919789-77-8

Reaction Conditions

1.1 Reagents: Boron tribromide Solvents: Dichloromethane ;  -78 °C; -78 °C → rt; 16 h, rt
1.2 Reagents: Water

Reference

Self-Assembly of Tetraphenylethene-Based [2]Catenane Driven by Acid-Base-Controllable Molecular Switching and Its Enabled Aggregation-Induced Emission

Ramakrishnam Raju, Mandapati V.; Lin, Hong-Cheu, Organic Letters, 2014, 16(21), 5564-5567

Production Method 11

919789-77-8

Reaction Conditions

1.1 Reagents: p-Toluenesulfonic acid Solvents: Toluene ;  2.5 h, reflux

Reference

Method for identifying and resolving chiral compounds using AIE molecules

, China, , ,

Production Method 12

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  cooled; overnight, 70 °C; 70 °C → rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  rt

Reference

Multi-Stimuli Responsive FRET Processes of Bifluorophoric AIEgens in an Amphiphilic Copolymer and Its Application to Cyanide Detection in Aqueous Media

Nhien, Pham Quoc; Chou, Wei-Lun; Cuc, Tu Thi Kim; Khang, Trang Manh; Wu, Chia-Hua; et al, ACS Applied Materials & Interfaces, 2020, 12(9), 10959-10972

Production Method 13

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  0 °C; 2 h, reflux
1.2 Solvents: Tetrahydrofuran ;  3 h, reflux

Reference

Design and synthesis of Norendoxifen analogues with dual aromatase inhibitory and estrogen receptor modulatory activities

Lv, Wei; Liu, Jinzhong; Skaar, Todd C.; Flockhart, David A.; Cushman, Mark, Journal of Medicinal Chemistry, 2015, 58(6), 2623-2648

Production Method 14

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  -10 °C; -10 °C → rt; 2 h, 90 °C; cooled
1.2 Solvents: Tetrahydrofuran ;  3 h, 90 °C
1.3 Reagents: Potassium carbonate Solvents: Water ;  0 °C

Reference

Novel ridaifen analog, method for producing same, and antitumor agent

, World Intellectual Property Organization, , ,

Production Method 15

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  0 °C; 6 h, rt → reflux
1.2 Reagents: Hydrochloric acid Solvents: Water

Reference

Redox-Active AIEgen-Derived Plasmonic and Fluorescent Core@Shell Nanoparticles for Multimodality Bioimaging

He, Xuewen ; Zhao, Zheng; Xiong, Ling-Hong; Gao, Peng Fei; Peng, Chen; et al, Journal of the American Chemical Society, 2018, 140(22), 6904-6911

Production Method 16

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  0 °C; 0.5 h, rt; 5 h, reflux
1.2 Reagents: Water

Reference

Aggregation-Induced Emission Materials with Narrowed Emission Band by Light-Harvesting Strategy: Fluorescence and Chemiluminescence Imaging

Zhu, Xin; Wang, Jian-Xin; Niu, Li-Ya ; Yang, Qing-Zheng, Chemistry of Materials, 2019, 31(9), 3573-3581

Production Method 17

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  -10 °C; -10 °C → rt; 0.5 h, rt; rt → 75 °C; 12 h, 75 °C

Reference

Preparation and application of sodium tetrastyryl disulfonate

, China, , ,

Production Method 18

119-61-9

611-99-4

919789-77-8

Reaction Conditions

1.1 Reagents: Zinc ,  Titanium tetrachloride Solvents: Tetrahydrofuran ;  10 min, rt; overnight, reflux

Reference

Phenol-yne Click Polymerization: An Efficient Technique to Facilely Access Regio- and Stereoregular Poly(vinylene ether ketone)s

Shi, Yang; Bai, Tianwen; Bai, Wei; Wang, Zhe; Chen, Ming; et al, Chemistry - A European Journal, 2017, 23(45), 10725-10731

Production Method 19

90-96-0

101-81-5

919789-77-8

Reaction Conditions

1.1 Reagents: Butyllithium Catalysts: p-Toluenesulfonic acid Solvents: Tetrahydrofuran ;  6 h, rt

Reference

Transparent thermoplastic copolymer with excellent heat resistance and impact strength and its manufacturing method

, Korea, , ,

Production Method 20

68161-05-7

919789-77-8

Reaction Conditions

1.1 Reagents: Boron tribromide Solvents: Dichloromethane ,  Water ;  24 h, rt

Reference

Sulfonated poly(ether sulfone) polymer electrolyte membrane containing metallophthalocyanine and method for manufacturing the same

, Korea, , ,

DHTPE Raw materials

• Benzophenone
• 4,4'-Dimethoxybenzophenone
• Benzene, 1,1'-(diphenylethenylidene)bis[4-methoxy-
• Bis(4-hydroxy)benzophenone
• benzylbenzene

DHTPE Preparation Products

• DHTPE (919789-77-8)

• 1. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
• 2. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 3. Dissolved oxygen sensor based on fluorescence quenching of oxygen-sensitive ruthenium complexes immobilized in sol–gel-derived porous silica coatings
  Analyst, 1996,121, 785-788
• 4. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?
  Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
• 5. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147

• Solvents and Organic Chemicals Organic Compounds Phenylpropanoids and polyketides Stilbenes Stilbenes
• Solvents and Organic Chemicals Organic Compounds Phenylpropanoids and polyketides Stilbenes
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

• 66422-18-2(1,1-bis(4-hydroxyphenyl)-2-phenylethylene)
• 919789-89-2(Phenol, 4-(1-methyl-2-phenyl-1-propen-1-yl)-)
• 61064-71-9(Phenol, 4,4'-(1-phenyl-1,2-ethenediyl)bis[2,6-dimethyl-)
• 13366-36-4(Phenol,4,4'-(1,2-dimethyl-1,2-ethenediyl)bis-)
• 61064-72-0(Phenol, 4,4'-(phenylethenylidene)bis[2,6-dimethyl-)
• 919789-82-5(Phenol, 4-(1-methyl-2,2-diphenylethenyl)-)
• 82925-28-8((Z,E)-1,2-DIPHENYL-1-(4-HYDROXYPHENYL)ETHENE)
• 552-80-7(Phenol,4,4'-[(1E)-1,2-dimethyl-1,2-ethenediyl]bis-)
• 68578-79-0(Phenol, 4,4'-(1,2-diphenyl-1,2-ethenediyl)bis-)
• 76115-06-5(4-(1,2,2-Triphenylvinyl)phenol)