SU794005A1 - 3-(4-bromophenyl)-10-hydroxy-1-carboxybenzo/f/quinooline sulfonic-8 acid possessing analytical luminescent reagent properties - Google Patents

3-(4-bromophenyl)-10-hydroxy-1-carboxybenzo/f/quinooline sulfonic-8 acid possessing analytical luminescent reagent properties Download PDF

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SU794005A1
SU794005A1 SU792751658A SU2751658A SU794005A1 SU 794005 A1 SU794005 A1 SU 794005A1 SU 792751658 A SU792751658 A SU 792751658A SU 2751658 A SU2751658 A SU 2751658A SU 794005 A1 SU794005 A1 SU 794005A1
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SU
USSR - Soviet Union
Prior art keywords
carboxybenzo
bromophenyl
hydroxy
quinooline
sulfonic
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SU792751658A
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Russian (ru)
Inventor
Виталий Иванович Летунов
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Читинский Государственный Педаго-Гический Институт Им.H.Г.Чернышевского
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Priority to SU792751658A priority Critical patent/SU794005A1/en
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Publication of SU794005A1 publication Critical patent/SU794005A1/en

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Description

гаетс , что св зано с его пол рностью (представл ет собой внутреннюю соль). Дополнительно может быть очищено перекристаллизацией из смеси ДМСО - изобутанол 1:1. Элементный анализ:supposed to be due to its polarity (it is an internal salt). Additionally, it can be purified by recrystallization from a mixture of DMSO - isobutanol 1: 1. Elemental analysis:

Найдено, %: С 50,5; Н 1,9; N 2,6.Found,%: C 50.5; H 1.9; N 2.6.

CzoHiaBrNOeS.CzoHiaBrNOeS.

Вычислено, %: С 51,25; Н 2,56; N 2,99.Calculated,%: C, 51.25; H 2.56; N 2.99.

Возможность применени  предлагаемого соединени  в качестве люминесцентного реагента на магний исследуют на примере изучени  люминесценции водных растворов этого соединени  при различных значени х рН в присутствии различных катионовThe possibility of using the proposed compound as a luminescent reagent for magnesium is investigated using the example of studying the luminescence of aqueous solutions of this compound at different pH values in the presence of various cations.

(К+, Na, Са2ь, Ba2 Sr, , Mg2 А13+, Fe2+, РеЗг, Со, Ni, , ,(K +, Na, Ca2b, Ba2Sr,, Mg2A13 +, Fe2 +, ReZg, Co, Ni,,,

Hg2, , Zif+, Cu2+, Ag+).Hg2, Zif +, Cu2 +, Ag +).

При этом получают следующие результаты:The following results are obtained:

1)собственна  люминесценци  вещества в водном растворе:1) intrinsic luminescence of a substance in an aqueous solution:

рН менее 2,5 Ярка  зелена ; 2,5-6,5 Ярка  голуба ; 6,5-7,5 Темно-голуба  средней силы; Более 7,5 Практически отсутствует;pH less than 2.5 Bright green; 2.5-6.5 Bright blue; 6.5-7.5 Dark blue of medium strength; Over 7.5 Virtually absent;

2)в присутствии вышеперечисленных катионов в кислой среде характер люминесценции не измен етс ;2) in the presence of the above cations in an acidic medium, the nature of the luminescence does not change;

3)в щелочной среде в присутствии выщеперечисленных катионов за исключением магни  люминесценци  отсутствует. В присутствии магни  возникает розова  люминесценци  средней силы;3) in an alkaline medium in the presence of the above cations, with the exception of magnesium, there is no luminescence. In the presence of magnesium, pink luminescence of medium strength occurs;

4)существует пр ма  зависимость силы люминесценции от концентрации магни . Закон Бера соблюдаетс  дл  концентраций магни  до 8 мкг/мл. Выще этой концентрации реагент образует с магнием нерастворимый осадок;4) there is a direct dependence of the luminescence force on the magnesium concentration. Bera's law is observed for magnesium concentrations up to 8 µg / ml. Above this concentration, the reagent forms an insoluble precipitate with magnesium;

5)все вышеперечисленные катионы не мешают определению магни  за исключением тех случаев, когда образуют в щелочной среде плотные осадки.5) all of the above cations do not interfere with the determination of magnesium, unless they form dense precipitates in an alkaline medium.

В качестве примера количественного определени  магни  изучено определение магни  в основах: всех основ растворено по 0,1 г в 45 мл 0,1 Н. раствора NaOH. Магни  введено по 5,0 мл 0,001 н. раствора (получено содержание 2,4 мкг/мл). Реагент вводилс  по 0,1 мл 0,01%-ного раствора в 0,1 н. растворе NaOH.As an example of the quantitative determination of magnesium, the definition of magnesium in the bases was studied: all bases were dissolved in 0.1 g in 45 ml of 0.1 N. NaOH solution. Magni is administered in 5.0 ml 0.001 n. solution (obtained content of 2.4 µg / ml). The reagent was injected at 0.1 ml of 0.01% solution in 0.1 n. NaOH solution.

Люминесцен- Найдено, ци , %мкл/млLuminesce- Found, qi,% μl / ml

3535

2,6 2.6

34,5 2,4 34.5 2.4

34,0 2,2 34.0 2.2

35,0 2,6 35.0 2.6

35,5 2,935.5 2.9

Относительна  ошибка 5%.The relative error is 5%.

Таким образом, 3-(4-бромфенил)-10-окси1 - карбоксибензо / хинолинсульфонова -8 кислота  вл етс  высокоспецифичным реагентом на магний.Thus, 3- (4-bromophenyl) -10-hydroxy-carboxybenzo / quinoline sulfonic acid is a highly specific reagent for magnesium.

Claims (2)

1.Реагенты дл  люминесцентного анализа . М., ИРЕА, 1971, с. 5.1. Reagents for luminescence analysis. M., IREA, 1971, p. five. 2.Козлов Н. С. 5,6-Бензохинолины, Минск, «Наука и техника, 1970.2. Kozlov, N. S. 5,6-Benzoquinolines, Minsk, “Science and Technology, 1970.
SU792751658A 1979-04-13 1979-04-13 3-(4-bromophenyl)-10-hydroxy-1-carboxybenzo/f/quinooline sulfonic-8 acid possessing analytical luminescent reagent properties SU794005A1 (en)

Priority Applications (1)

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SU792751658A SU794005A1 (en) 1979-04-13 1979-04-13 3-(4-bromophenyl)-10-hydroxy-1-carboxybenzo/f/quinooline sulfonic-8 acid possessing analytical luminescent reagent properties

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU792751658A SU794005A1 (en) 1979-04-13 1979-04-13 3-(4-bromophenyl)-10-hydroxy-1-carboxybenzo/f/quinooline sulfonic-8 acid possessing analytical luminescent reagent properties

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008125628A3 (en) * 2007-04-13 2009-04-09 Basf Se Method for the formation of organic pigments

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008125628A3 (en) * 2007-04-13 2009-04-09 Basf Se Method for the formation of organic pigments

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