Patent classifications
C07F7/2284
Process for preparing organotin compounds
Provided is an efficient and effective process for preparing certain organotin compounds having alkyl and alkylamino substituents. The process provides the organotin compounds in a highly pure crystalline form which are particularly useful as precursors in the deposition of high-purity tin oxide films in, for example, extreme ultraviolet light (EUV) lithography techniques used in the manufacture of certain microelectronic devices.
Anode for lithium ion secondary battery and lithium ion secondary battery
A lithium ion secondary battery includes a cathode, an anode, and an electrolytic solution. The anode includes a cyclic compound and the cyclic compound includes one or more of a first cyclic compound, a second cyclic compound, and a third cyclic compound.
Symmetric Charge Transfer Compounds for Organic Photovoltaics
The present disclosure is related to organic acceptor-donor-acceptor compounds as non-fullerene acceptors for use in organic photovoltaics.
PHOTORESIST FOR SEMICONDUCTOR FABRICATION
An organometallic precursor for extreme ultraviolet (EUV) lithography is provided. An organometallic precursor includes an aromatic di-dentate ligand, a transition metal coordinated to the aromatic di-dentate ligand, and an extreme ultraviolet (EUV) cleavable ligand coordinated to the transition metal. The aromatic di-dentate ligand includes a plurality of pyrazine molecules.
METHODS TO PRODUCE ORGANOTIN COMPOSITIONS WITH CONVENIENT LIGAND PROVIDING REACTANTS
Synthesis reactions are described to efficiently and specifically form compounds of the structure RSnL3, where R is an organic ligand to the tin, and L is hydrolysable ligand or a hydrolysis product thereof. The synthesis is effective for a broad range of R ligands. The synthesis is based on the use of alkali metal ions and optionally alkaline earth (pseudo-alkaline earth) metal ions. Compounds are formed of the structures represented by the formulas RSn(C≡CSiR′.sub.3).sub.3, R′R″ACSnL.sub.3, where A is a halogen atom (F, Cl, Br or I) or an aromatic ring with at least one halogen substituent, R′R″(R′″O)CSnL.sub.3 or R′R″(N≡C)CSnZ.sub.3.
COMPOSITIONS AND RELATED METHODS OF ALKYLTINTRIHALIDES
The present disclosure includes a method of obtaining an alkyltintrihalide, obtaining a solvent, and contacting the alkyltintrihalide and the solvent, thereby forming an alkyltintrihalide adduct. Also described is a composition including: an alkyltintrihalide adduct of the formula: RSnX.sub.3.Math.(solv).sub.n, wherein: R is a substituted C.sub.1-C.sub.5 alkyl, an unsubstituted C.sub.1-C.sub.5 alkyl, a substituted C.sub.1-C.sub.5 alkenyl, or an unsubstituted C.sub.1-C.sub.5 alkenyl; X is Cl, Br, or I; solv is a solvent; and n is at least 1.
HIGH PURITY ALKYL TIN COMPOUNDS AND MANUFACTURING METHODS THEREOF
Monoalkyl tin triamide compounds having purity of at least about 99 mol % and the chemical formula RSn(NMe.sub.2).sub.3 are described. R.sup.1 is selected from R.sup.A, R.sup.B, and R.sup.C; R.sup.A is a primary alkyl group having about 1 to 10 carbon atoms, R.sup.B is a secondary alkyl group having about 3 to 10 carbon atoms, and R.sup.C is a tertiary alkyl group having about 3 to 10 carbon atoms; each R.sup.2 is independently an alkyl group having about 1 to 10 carbon atoms; and a content of R.sup.1Sn(NR.sup.2.sub.2).sub.2(N(R.sup.2)CH.sub.2NR.sup.2.sub.2) is less than about 1 mol %. Methods for synthesizing, purifying, and storing these compounds are also provided. The monoalkyl tin compounds may be used for the formation of high-resolution EUV lithography patterning precursors and are attractive due to their high purity and minimal concentration of dialkyl tin and other tin impurities.
P-type organic semiconductor, composition, photoelectric conversion film, photoelectric conversion device, and image sensor
Provided are a p-type organic semiconductor represented by Chemical Formula (1), which has improved thermal resistance and may detect near-infrared light, and a photoelectric conversion film, a photoelectric conversion device, and an image sensor including the same: ##STR00001## In Chemical Formula (1), R.sub.1 and R.sub.2 are independently a substituted or unsubstituted C1 to C30 alkyl group, and R.sub.3 to R.sub.26 are independently a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted alkylthio group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted arylthio group, an oxy group substituted with a substituted or unsubstituted heterocyclic group, a thio group substituted with a substituted or unsubstituted heterocyclic group, or a substituted or unsubstituted amino group.
METHOD OF FORMING AND SEPARATING TIN(II) FROM TIN(IV)
Tin(IV)-117m is reduced by an acidic antimony solution to tin(II)-117m. A chelant is added to the solution of tin(II)-117m, and the pH is raised, forming tin(II)-117m chelant complex. The chelant is a bifunctional chelant, preferably attached to a bioactive molecule and reacted with the tin(II)-117m to form a radiopharmaceutical.
High-purity large-scale preparation of stannsoporfin
Large scale (bulk) compositions comprising high-purity stannsoporfin are disclosed, as well as methods of synthesizing such compositions.