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14916-87-1

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  • Factory Price OLED 99% 14916-87-1 Copper(ll) 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecafluoro-29H,31H-phthalocyanine Manufacturer

    Cas No: 14916-87-1

  • USD $ 0.1-0.1 / Gram

  • 1 Gram

  • 100 Metric Ton/Year

  • Xi'an Xszo Chem Co., Ltd.
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  • 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-Hexadecafluorophthalocyanine copper(II)

    Cas No: 14916-87-1

  • USD $ 1.2-5.0 / Kiloliter

  • 5 Kiloliter

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  • Chemwill Asia Co., Ltd.
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14916-87-1 Usage

Description

COPPER 1 2 3 4 8 9 10 11 15 16 17 18 22&, also known as Copper(II) 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecafluoro-29H,31H-phthalocyanine (CAS# 14916-87-1), is an organometallic complex with a unique structure that provides it with various applications in different industries. It is characterized by its electron transporting properties, good air-stability, and an electron mobility of 0.11 cm2/Vs.

Uses

Used in Photodetector Applications:
COPPER 1 2 3 4 8 9 10 11 15 16 17 18 22& is used as an organic photodetector for near-IR light, making it suitable for applications where detection of light in the near-infrared spectrum is required.
Used in Catalyst Applications:
COPPER 1 2 3 4 8 9 10 11 15 16 17 18 22& functions as a catalyst that facilitates the electrochemical reduction of carbon dioxide to ethylene in aqueous media, contributing to the development of sustainable chemical processes.
Used in Energy Conservation Applications:
COPPER 1 2 3 4 8 9 10 11 15 16 17 18 22& is used as an electron transporting layer for semiconducting applications, such as an electron accepting material for organic photovoltaic cells. This contributes to the development of energy-efficient and environmentally friendly solar cells.
Used in Electronics Industry:
COPPER 1 2 3 4 8 9 10 11 15 16 17 18 22& is used in the fabrication of organic thin film transistors (OTFTs) and quartz crystal microbalance (QCM) based sensors, enhancing the performance and efficiency of these devices.
Used in Research and Development:
COPPER 1 2 3 4 8 9 10 11 15 16 17 18 22& is used as a catalyst in biomimetic sensors, aiding in the development of innovative and sensitive detection methods for various applications in research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 14916-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14916-87:
(7*1)+(6*4)+(5*9)+(4*1)+(3*6)+(2*8)+(1*7)=121
121 % 10 = 1
So 14916-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C32F16N8.Cu/c33-9-1-2(10(34)18(42)17(9)41)26-49-25(1)53-27-3-4(12(36)20(44)19(43)11(3)35)29(50-27)55-31-7-8(16(40)24(48)23(47)15(7)39)32(52-31)56-30-6-5(28(51-30)54-26)13(37)21(45)22(46)14(6)38;/q-2;+2/rC32CuF16N8/c34-9-1-2(10(35)18(43)17(9)42)26-50-25(1)52-29-5-6(14(39)22(47)21(46)13(5)38)31-54-27-3-4(12(37)20(45)19(44)11(3)36)28(51-27)55-32-8-7(15(40)23(48)24(49)16(8)41)30(53-26)57(32)33-56(29)31/b52-25-,52-29-,53-26-,53-30-,54-27-,54-31-,55-28-,55-32-

14916-87-1 Well-known Company Product Price

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  • Aldrich

  • (446653)  Copper(II)1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecafluoro-29H,31H-phthalocyanine  Dye content 80 %

  • 14916-87-1

  • 446653-1G

  • 1,389.96CNY

  • Detail

14916-87-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-Hexadecafluorophthalocyanine Copper(II)

1.2 Other means of identification

Product number -
Other names COPPER 1 2 3 4 8 9 10 11 15 16 17 18 22&

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14916-87-1 SDS

14916-87-1Downstream Products

14916-87-1Relevant articles and documents

Photon assisted-inversion of majority charge carriers in molecular semiconductor-based organic heterojunctions

Kikobo, Gracia Loma,Kumar, Abhishek,Vibhu, Vaibhav,Ouedraogo, Seydou,Deshotel, Alix,Mateos, Micka?l,Meunier-Prest, Rita,Bouvet, Marcel

, p. 5008 - 5020 (2021)

Ambipolar molecular materials hold great promise as a building block of next generation highly efficient, less complex and low cost electronic devices. In this endeavor, the present work reports the fabrication of organic heterojunction devices based on halogenated copper phthalocyanine (CuPc) and lutetium bisphthalocyanine (LuPc2) bilayers, investigates their structural and electrical properties and probes the ambipolar behavior by ammonia sensing. Microstructural analysis of the heterostructure thin films revealed compact and semicrystalline organization, depending on the number of halogen substituents in CuPc. The heterojunction devices reveal non-linear I(V) characteristics associated with an interfacial energy barrier which is tuned by the number and type of halogen substituents. The behavior of the devices towards NH3 exposure revealed n-type, p-type and ambipolar transport depending on 16, 0 and 8 fluorine substituents, respectively, present in the CuPc component of the heterostructure, demonstrating a correlation between the electronic effects of substituents and the thin film electrical properties. The trigger of the ambipolar transport regime in the heterojunction device is the visible light, such that the device conduction channel is dominated by holes in the dark and electrons under illumination. In depth charge transport studies by impedance spectroscopy explain the device electrical behavior and highlight the important role played by the interface in the heterostructures. Different charge transport parameters are extracted by fitting the experimental Nyquist curves, analysis of those confirms the presence of bulk and interfacial transport and provides an interpretation of the observed ambipolarity.

Synthesis, spectral characterization of CuPcF16 and its application in organic thin film transistors using p-6p as inducing layer

Ma, Feng,Wang, Shirong,Li, Xianggao

, p. 589 - 592 (2012)

An air-stable n-channel semiconductor material, CuPcF16, was synthesized in a slightly modified procedure and characterized by infrared (IR), X-ray diffraction (XRD), UVvis and fluorescence spectra. CuPcF16 showed a monomer character

Zeolite encapsulated cobalt(II) and copper(II) perfluorophthalocyanines. Synthesis and characterization

Balkus Jr., Kenneth J.,Gabrielov, Alexei G.,Bell, Stephen L.,Bedioui, Fethi,Roué, Lionel,Devynck, Jacques

, p. 67 - 72 (2008/10/08)

Synthetic faujasite type zeolites have been modified with cobalt(II) and copper(II) hexadecafluorophthalocyanines (MF16Pc) by synthesizing zeolite NaX around the MF16Pc complexes and by the template synthesis of the complexes inside NaY zeolites ion exchanged with Co2+ and Cu2+. Mid FT-IR and UV-vis spectroscopy as well as X-ray powder diffraction and elemental analysis provide evidence for the encapsulation of the MF16Pc complexes inside the zeolites. The redox properties of the intrazeolite metal complexes were investigated by cyclic voltammetry. Site isolation of these complexes inside the zeolite has resulted in electrochemical data for Co(II)/Co(I) and Cu(II)/ Cu(I) redox processes not observed in solution.

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