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germanium(IV) phthalocyanine dichloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19566-97-3 Structure
  • Basic information

    1. Product Name: germanium(IV) phthalocyanine dichloride
    2. Synonyms: germanium(IV) phthalocyanine dichloride;Dichloro(phthalocyanine)germanium;Dichlorogermanium phthalocyanine;Phthalocyanine germanium(IV)chloride
    3. CAS NO:19566-97-3
    4. Molecular Formula: C32H16Cl2GeN8
    5. Molecular Weight: 656.07
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19566-97-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: germanium(IV) phthalocyanine dichloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: germanium(IV) phthalocyanine dichloride(19566-97-3)
    11. EPA Substance Registry System: germanium(IV) phthalocyanine dichloride(19566-97-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 19566-97-3(Hazardous Substances Data)

19566-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19566-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,6 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19566-97:
(7*1)+(6*9)+(5*5)+(4*6)+(3*6)+(2*9)+(1*7)=153
153 % 10 = 3
So 19566-97-3 is a valid CAS Registry Number.

19566-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Cl2-Ge(phthalocyanine)

1.2 Other means of identification

Product number -
Other names (phthalocyanine)GeCl2

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:19566-97-3 SDS

19566-97-3Relevant articles and documents

Germanium triazatetrabenzcorrole and germanium phthalocyanine: Synthesis, fluorescence and singlet oxygen generation

Zhang, Xian-Fu,Sun, Xiaojie

, p. 847 - 852 (2018)

The synthesis, fluorescence properties and singlet oxygen generation capability of germanium tetrabenzotriazacorrole (LGeTBC), germanium phthalocyanine (Cl2GePc) and their derivatives are described. Measurements include UV-vis absorption spectra, fluoresc

PHTHALOCYANINE PIGMENT, COLORING COMPOSITION AND COLOR FILTER

-

Paragraph 0179, (2017/11/15)

PROBLEM TO BE SOLVED: To provide a phthalocyanine pigment that has excellent fastness (heat resistance, light fastness, solvent resistance) and, when used for a color filter or the like, is excellent in color properties (lightness) and the contrast ratio, without causing unusual matter due to association, aggregation or the like of molecules with each other even in a high temperature environment above 230°C. SOLUTION: The invention provides: a phthalocyanine pigment having a specific structure represented by general formula (1) or the like; and a coloring composition and a color filter using the phthalocyanine pigment. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Two isomorphous complexes: Dichloro[phthalocyaninato(2-)]tin(IV) and dichloro[phthalocyaninato(2-)]-germanium(IV)

Janczak, Jan,Kubiak, Ryszard

, p. m237-m240 (2007/10/03)

Isomorphous triclinic forms of dichloro[phthalocyaninato(2-)]tin(IV), [Sn(C32H16N8)Cl2], and dichloro[phthalocyaninato(2-)]germanium(IV), [Sn(C32H16N8)Cl2], and a monoclinic form of the latter have been obtained from the reaction of pure tin and germanium powder, respectively, with phthalonitrile under a stream of ICl vapour. All three crystal structures consist of centrosymmetric [SnPcCl2] and [GePcCl2 [Pc is phthalocyaninate(2-)] molecules, which are separated but interacting. In the triclinic forms (Sn and Ge), the Pc macrocycles are not staggered but slipped, and in the monoclinic form (Ge), the molecules are additionally inclined. In both cases, the central Sn or Ge atom is six-coordinated by the four isoindole N atoms of the Pc macrocyclic ligand and by two Cl atoms (located trans) into a tetragonal-bipyramidal structure. The arrangement of [SnPcCl2] and [GePcCl2] molecules in the crystal structure is determined mainly by intermolecular C-H...Cl, π-π and van der Waals interactions.

Synthesis and Properties of (Phthalocyaninato)germanium Sulfur Compounds

Fischer, Konrad,Hanack, Michael

, p. 1860 - 1865 (2007/10/02)

PcGe(OH)2 (7) reacts with thiophenol and 4-methylthiophenol to form the (phthalocyaninato)germanium sulfur compounds PcGe(SR)2 (5a and b).A product with the composition n (2) was obtained in two ways: By the reaction of 7 with H2S under pressure and through the reaction of 7 with triphenylsilanethiol (9).In comparison with n (1b) polycrystalline samples of 2 do not show a pronounced increase of electrical conductivity.

Cofacial Assembly of Partially Oxidized Metallomacrocycles as an Approach to Controlling Lattice Architecture in Low-Dimensional Molecular Solids. Chemical and Architectural Properties of the "Face-to-Face" Polymers n, Where M = Si, Ge, and Sn

Dirk, Carl W.,Inabe, Tamotsu,Schoch, Karl F.,Marks, Tobin J.

, p. 1539 - 1550 (2007/10/02)

This contribution reports a detailed chemical, spectroscopic, and X-ray diffractometric study of the nature and structure of the cofacially joined metallomacrocyclic polymers n, where M = Si, Ge, Sn and Pc = phtalocyaninato.These materials are precursors for a new class of electrically conductive polymers.Improved syntheses of the polymers are first reported.Optical spectra are assigned within the context of a porphyrinic "four orbital" model and related to those of the corresponding M(Pc)Cl2 and M(Pc)(OH)2 monomers.The vibrational spectra of the polymers are assigned, employing data from the aforementioned monomers and 18O substitution.Identification of the M-O stretching modes allows an estimation of the polymer molecular weights as a function of polymerization procedure via an end group analysis.Degrees of polymerization obtained for typical samples are n = 120 (30) (M = Si), 70 (40) (M = Ge), 100 (40) (M = Sn).A parallel, radiotracer determination employing labeled M(Pc)(O3H)2 monomers yields results in favorable agreement.It is found that n can be substantially varied by controlling the polymerization conditions.X-ray diffraction measerements show the n polymers to be highly crystalline.An analysis of the powder X-ray diffraction data has been carried out with carefully selected model compounds and computer simulation techniques.The results are in good accord with the proposed structure consisting of parallel chains of cofacially arrayed metallomacrocycles.The simplest structures which fit the experimental data are as follows: n, orthorhombic space group Ibam, a = 13.80 (5) Angstroem, b = 27.59 (5) Angstroem, c = 6.66 (4) Angstroem, Z = 4, interplanar spacing = 3.33 (2) Angstroem, intrastack phthalocyanine staggering angle = 39 (3) deg, density (g cm-3) = 1.458 (21) (calcd), 1.432 (10) (found); n, tetragonal space group P4/m, a = 13.27 (5) Angstroem, c = 3.53 (2) Angstroem, Z = 1, interplanar spacing = 3.53 (2) Angstroem, intrastack phthalocyanine staggering angle = 0 (5) deg, density (g cm-3) = 1.609 (29) (calcd), 1.512 (19) (found), or tetragonal space group I4/m, a = 18.76 (7) Angstroem, c = 3.53 (2) Angstroem, Z = 2, intrastack phthalocyanine staggering angle = 0 (5) deg, density (g cm-3) = 1.589 (26) (calcd), 1.512 (10) (found); n, tetragonal space group P4/m, a = 12.82 (2) Angstroem, c = 3.83 (2) Angstroem, Z = 1, intrastack phthalocyanine staggering angle ca. 0 deg, density (g cm-3) = 1.712 (25) (calcd), 1.719 (10) (found).The data for the latter structure are best fit to a model where the larger size of the Sn(IV) ion induces buckling of the macrocycle skeleton.An approximate analysis of the diffraction line widths suggests that crystallite dimensions are on the order of several hundred angstroms and are not grossly anisotropic.

SYNTHESIS AND PROPERTIES OF A NEW KIND OF ONE-DIMENSIONAL C0NDUCTOR VIII. SYNTHESIS AND CHARACTERIZATION OF trans-BIS-1-ALKYNYL SUBSTITUTED SILICON, GERMANIUM, TIN PHTHALOCYANINES AND GERMANIUM HEMIPORPHYRAZINES

Hanack, Michael,Mitulla, Konrad,Pawlowski, Georg,Subramanian, L. R.

, p. 315 - 326 (2007/10/02)

The preparation of several new trans-bis-1-alkynyl(phthalocyaninato)silicon (VIc-f), -germanium(VIIc-f) and -tin(VIIId,f) compounds as well as trans-bis-1-alkynyl(hemiporphyrazinato)germanium (XIc, e, f) derivatives is described.The products were obtained

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