25510-41-2

Usage

Uses

Used in Magnetic Applications:
Dilithium phthalocyanine is used as a precursor for the development of single-molecule magnets (SMMs) by coordinating with lanthanide metals. These SMMs exhibit unique magnetic properties, such as slow magnetic relaxation and quantum tunneling of magnetization, which are of great interest for advanced magnetic storage, quantum computing, and molecular spintronics applications.
Used in Chemical Synthesis:
Dilithium phthalocyanine can be employed as a starting material or intermediate in the synthesis of various complex organic compounds, particularly those involving phthalocyanine derivatives. Its unique structure and reactivity make it a valuable building block for the development of novel materials with tailored properties for specific applications.
Used in Material Science:
The compound's ability to coordinate with lanthanide metals and its magnetic properties make it a potential candidate for the development of advanced materials with enhanced magnetic, optical, and electronic properties. These materials could find applications in various fields, such as sensors, displays, and energy conversion devices.
Used in Pharmaceutical Research:
Although not explicitly mentioned in the provided materials, the unique properties of Dilithium phthalocyanine may also make it a promising candidate for pharmaceutical research. Its ability to coordinate with metal ions and its potential applications in material science could lead to the development of new drugs or drug delivery systems with improved efficacy and selectivity.

InChI:InChI=1/C32H18N8.2Li/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25;;/h1-16H,(H2,33,34,35,36,37,38,39,40);;/q;2*+1

Upstream product

• 91-15-6 phthalonitrile 
• 574-93-6 29H,31H-Phthalocyanine 

Relevant academic research and scientific papers

Phthalocyanine-based molecular paramagnets. Effect of double-decker structure on magnetothermal properties of gadolinium complexes

Gadolinium is useful in the room temperature magnetic refrigeration due to its large magnetocaloric effect occurring at temperatures close to room. We predict and represent known phthalocyanine complexes as a new class of paramagnets with a large magnetocaloric effect at the temperatures close to room acting due to gadolinium atom located in a coordination site of a conjugated phthalocyanine macrocycle/macrocycles. Magnetothermal properties (a magnetocaloric effect, specific heat capacity, heat released due to MCE, enthalpy/entropy change) of paramagnetic (AcO)GdPc and GdPc2[Formula presented], Pc – phthalocyanine dianion, as the 3% water suspensions at 278–338?K in the magnetic fields of 0–1.0?T were studied for the first time in the family of these paramagnets. The study of magnetothermal properties and specific heat capacity were performed in two independent experiments by microcalorimetry and differential scanning calorimetry, respectively. Large positive MCE in (AcO)GdPc reaches a value of 0.47?K at 278?K when the magnetic field is changed from 0 to 1?T. MCE in [Formula presented] is lower by almost an order of magnitude compared with (AcO)GdPc, which indicates that the intramolecular oxidation-activated spin coupling does not prevail over the intermolecular coupling of two radical spins.

Sandwich complexes of yttrium, neodymium, gadolinium, and dysprosium with meso-trans-di(hexadecyl)-tetrabenzoporphyrin and phthalocyanine fragments. Synthesis and spectral properties

Sandwich-type asymmetric complexes of yttrium, neodymium, gadolinium, and dysprosium were synthesized by the reaction of the corresponding meso-trans-bis(hexadecyl)tetrabenzoporphyrinates with dilithium phthalocyianine. Spectral properties of these compou

Anchoring of rare-earth-based single-molecule magnets on single-walled carbon nanotubes

A new heteroleptic bis(phthalocyaninato) terbium(III) complex 1, bearing a pyrenyl group, exhibits temperature and frequency dependence of ac magnetic susceptibility, typical of single-molecule magnets. The complex was successfully attached to single-wall

Red-emitting organic electroluminescent device

Disclosed is a red-emitting organic electroluminescent device comprising in sequence an anode, an organic hole injecting and transporting zone, a doped luminescent zone, an electron transport zone and a cathode, characterized in that said doped luminescent zone is comprised of a fluorescent phthalocyanine compound capable of emitting a wavelength in the range of 660 to 780 nm.