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1)  Calix[4]arene biradical with two nitroxides
杯[4]芳烃双氮氧自由基
2)  Azocalix[4]arene
偶氮基杯[4]芳烃
1.
Synthesis and Azo-quinoid Tautomerizm of Azocalix[4]arene
偶氮基杯[4]芳烃化合物的合成及其偶氮-醌腙互变异构性质
3)  biscalix[4]arene
双杯[4]芳烃
1.
Reacting 1,3-bis[2-(p-formylphenoxy)ethyloxy]-p-tert-butylcalix[4]arene 2 with 1,3-di(hydra- zinocarbonylmethoxy)-p-tert-butylcalix[4]arene 4 by 1+1 intermolecular condensation under diluted condi- tion, a novel biscalix[4]arene derivative 5 containing Schiff base and amide units was prepared in high yield.
对叔丁基杯[4]芳烃-1,3-二醛基衍生物2与对叔丁基杯[4]-1,3-二酰肼衍生物4在稀释条件下进行“1+1”分子间缩合反应,高产率地合成了含席夫碱和酰胺单元的新型双杯[4]芳烃衍生物5。
2.
By reacting 1,3-bis[2-(p-formylphenyloxy)ethyloxy]-p-tert-butylcalix[4]arene (1) with salicylide hydrazone or hydrazine hydrate in a "1+2"or a "2+2" condensation mode, a novel calix[4]arene derivative 2 or a biscalix[4]arene 3 bridged by benzalazine groups was conveniently obtained in a yield of 84% or 81%, respectively.
对叔丁基杯[4]芳烃-1,3-二醛基衍生物1分别与水杨醛腙、水合肼进行"1+2"和"2+2"缩合反应,方便地合成了苄连氮基取代或桥联的新型杯[4]芳烃衍生物2和双杯[4]芳烃衍生物3,产率分别为84%和81%。
4)  26,28-dimethoxycalix[4]arene
26,28-二甲氧基杯[4]芳烃
1.
In this paper a novel compound 11,23-dihexanoyl-26,28-dimethoxycalix[4]arene was synthesized selectively from 26,28-dimethoxycalix[4]arene by Fries rearrangement with hexanoyl chloride,and the highest rate of the yield could reach 58.
以26,28-二甲氧基杯[4]芳烃为原料,经Fries重排反应,选择性地合成了杯[4]芳烃酚羟基对位的二酰化产物:11,23-二己酰基-26,28-二甲氧基杯[4]芳烃,收率最高可达58。
5)  aza-bridged calix[4]arene
氮杂杯[4]芳烃
1.
In this paper,we synthesized aza-bridged calix[4]arene and its derivation.
论文合成了氮杂杯[4]芳烃及其衍生物,并对其与黑索今、奥克托今的配合性能进行了研究。
6)  Calix[4]arene-biscrown-6
杯[4]芳烃双冠-6
1.
Coordination Chemistry of Calix[4]arene-biscrown-6 with Cs~+ in Solution;
溶液中杯[4]芳烃双冠-6与Cs~+配位化学研究
补充资料:一杯
1.指一杯的容量。 2.表示少量。 3.特指一杯酒。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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