White light emitting material, preparation method thereof, and application thereof

    公开(公告)号:US11581489B2

    公开(公告)日:2023-02-14

    申请号:US16945060

    申请日:2020-07-31

    摘要: A white light emitting material having a chemical structural formula represented by formula (I), a preparation method thereof and application thereof. The preparation method comprises subjecting tris(4-iodophenyl)amine and 4-methoxyphenylacetylene or tris(4-iodophenyl)amine and methyl 4-ethynylbenzoate to a coupling reaction under protection of a protective gas and catalysis of a Pd/Cu mixed catalyst, to obtain the white light emitting material. A novel temperature-sensitive light emitting material is synthesized through a one-step method. The material is applied to the field of diode luminescence based on the temperature-sensitive characteristic. White light luminescence can be finally realized only by reasonably controlling the temperature and duration time during heating a substrate. Compared with the existing art, the method greatly saves raw material costs and manufacturing process costs, and provides a novel idea and strategy for use of a white organic light emitting diode.

    Process for manufacturing a complexing agent

    公开(公告)号:US11485703B2

    公开(公告)日:2022-11-01

    申请号:US16626026

    申请日:2018-06-19

    申请人: BASF SE

    IPC分类号: C07C227/26 C07C229/16

    摘要: The present invention is directed towards a process for manufacturing a complexing agent, said process comprising the steps of (a) Providing a nitrile according to general formula (I a) or (I b) With M being selected from alkali metal and hydrogen and combinations thereof, (b) Saponification with a total alkali amount of 2.5 to 2.9 mol of alkali metal hydroxide per mole of nitrile according to general formula (I a) or (I b), respectively, and a pH value in the range of from 9.5 to 11.5 at the end of step (b), (c) Adding an amount of alkali metal hydroxide so that the total alkali content is 2.9 to 3.15 moles per mole nitrile according to general formula (I a) or (I b), respectively, and (d) Allowing further conversion.

    Method of making (S)-3-(Aminomethyl)-5-Methylhexanoic acid
    8.
    发明授权
    Method of making (S)-3-(Aminomethyl)-5-Methylhexanoic acid 失效
    制备(S)-3-(氨基甲基)-5-甲基己酸的方法

    公开(公告)号:US5840956A

    公开(公告)日:1998-11-24

    申请号:US796159

    申请日:1997-02-06

    摘要: A method of making (.+-.)-3-(aminomethyl)-5-methylhexanoic acid that comprises condensing isovaleraldehyde with ##STR1## to form primarily ##STR2## reacting the ##STR3## with a cyanide source to form ##STR4## decarboxylating the ##STR5## to form ##STR6## hydrolyzing the ##STR7## with an alkali or alkaline earth metal hydroxide to form an alkali or alkaline earth metal carboxylate salt; and hydrogenating the alkali or alkaline earth metal carboxylate salt to form (.+-.)-3-(aminomethyl)-5-methylhexanoic acid, wherein R.sub.1 and R.sub.2 are the same or different and are hydrogen, C.sub.1 -C.sub.6 alkyl, aryl, benzyl, or C.sub.3 -C.sub.6 cycloalkyl. The present invention also provides a method of making (.+-.)-3-(aminomethyl)-5-methylhexanoic acid that comprises condensing isovaleraldehyde with ##STR8## to form primarily ##STR9## reacting the ##STR10## with a cyanide source to form ##STR11## decarboxylating the ##STR12## to form an alkali or alkaline earth metal carboxylate salt; and hydrogenating the alkali or alkaline earth metal carboxylate salt to form (.+-.)-3-(aminomethyl)-5-methylhexanoic acid.

    摘要翻译: 制备(+/-) - 3-(氨基甲基)-5-甲基己酸的方法,其包括将异戊醛与“IMAGE”缩合以主要形成以形成脱羧“IMAGE”以形成水解 使用碱金属或碱土金属氢氧化物形成碱金属或碱土金属羧酸盐的“IMAGE” 和氢化碱金属或碱土金属羧酸盐形成(+/-) - 3-(氨甲基)-5-甲基己酸,其中R 1和R 2相同或不同,为氢,C 1 -C 6烷基,芳基,苄基 ,或C 3 -C 6环烷基。 本发明还提供了制备(+/-) - 3-(氨基甲基)-5-甲基己酸的方法,其包括将异戊醛与“IMAGE”缩合以主要形成“IMAGE”,使“IMAGE”与氰化物源反应形成 使脱羧以形成碱金属或碱土金属羧酸盐; 并将碱金属或碱土金属羧酸盐氢化形成(+/-) - 3-(氨基甲基)-5-甲基己酸。

    Process for the preparation of N-substituted glycine acids or glycine
esters and the use of the process for indigo synthesis
    10.
    发明授权
    Process for the preparation of N-substituted glycine acids or glycine esters and the use of the process for indigo synthesis 失效
    用于制备N-取代的甘氨酸或甘氨酸酯的方法以及该方法用于靛蓝合成

    公开(公告)号:US5686625A

    公开(公告)日:1997-11-11

    申请号:US652445

    申请日:1996-06-05

    申请人: Carlo Kos

    发明人: Carlo Kos

    摘要: Process for the preparation of an N-substituted glycine ester or an N-substituted glycine acid by reaction of a glyoxylic acid ester half-acetal (hemiacetal) or glyoxylic acid half-acetal (hemiacetal) with an amine and hydrogenation of the intermediate product formed by this reaction, and the use of the process in a process for the preparation of indoxyl and indigo derivatives by cyclization of an N-arylglycine ester, prepared by the above process, in a molten alkali metal carbonate or alkaline earth metal carbonate with or without addition of an alkali metal amide, and if appropriate oxidation of the indoxyl derivative formed by this reaction to give the corresponding indigo derivative.

    摘要翻译: PCT No.PCT / EP94 / 04259 Sec。 371日期:1996年6月5日 102(e)日期1996年6月5日PCT 1994年12月21日PCT PCT。 公开号WO95 / 18093 日期1995年7月6日通过乙醛酸半缩醛(半缩醛)或乙醛酸半缩醛(半缩醛)与胺的反应和氢化反应制备N-取代的甘氨酸酯或N-取代的甘氨酸的方法 通过该反应形成的中间产物,以及该方法在制备吲哚氧基和靛蓝衍生物的方法中的用途,通过上述方法制备的N-芳基甘氨酸酯在熔融碱金属碳酸盐或碱土中 金属碳酸盐,加入或不加入碱金属氨化物,如果适当地氧化通过该反应形成的吲哚基衍生物,得到相应的靛蓝衍生物。