SU617465A1 - Complexes of bivalent iron with derivatives of 5-nitroso-6-oxyquinoline as dyes for natural and synthetic polyamide fibres - Google Patents

Complexes of bivalent iron with derivatives of 5-nitroso-6-oxyquinoline as dyes for natural and synthetic polyamide fibres

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Publication number
SU617465A1
SU617465A1 SU762404035A SU2404035A SU617465A1 SU 617465 A1 SU617465 A1 SU 617465A1 SU 762404035 A SU762404035 A SU 762404035A SU 2404035 A SU2404035 A SU 2404035A SU 617465 A1 SU617465 A1 SU 617465A1
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SU
USSR - Soviet Union
Prior art keywords
nitroso
dyes
oxyquinoline
derivatives
complexes
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SU762404035A
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Russian (ru)
Inventor
Тамара Михайловна Тимофеева
Елена Сергеевна Кузина
Лидия Михайловна Быкова
Андрей Васильевич Ельцов
Лидия Павловна Ковжина
Original Assignee
Ленинградский Ордена Трудового Красного Знамени Технологический Институт Им.Ленсовета
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Priority to SU762404035A priority Critical patent/SU617465A1/en
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Целевые продукты растворимы в диметилформамиде , пиридине, диметилсульфоксиде , разбавлепных минеральных кислотах . Ограниченно растворимы в спирте, ацетоне , ацетонитриле, гор чей воде.The target products are soluble in dimethylformamide, pyridine, dimethyl sulfoxide, dilute-mineral acids. Slightly soluble in alcohol, acetone, acetonitrile, hot water.

Новые красители окрашивают шерсть и полиамидные волокна из водных красильных ванн в интенсивные зеленые тона с прекрасными колористическими характеристиками , причем при окрашивании синтетических волокон исключаетс  необходимость применени  диспергатора.New dyes dye wool and polyamide fibers from aqueous dye baths in intense green tones with excellent color characteristics, and dyeing synthetic fibers eliminates the need for a dispersant.

Новые внутрикомплексные соединени  на основе нитрозооксихинолина позвол ют расширить цветную гамму и ассортимент отечественных красителей.New intracomplex compounds based on nitroso-oxyquinoline allow the color gamut and assortment of domestic dyes to be expanded.

Ниже приведены примеры синтеза новых внутрикомплексных соединений железа формулы (II) с производными 5-нитрозо-6-оксихинолина .Below are examples of the synthesis of new intracomplex iron compounds of formula (II) with 5-nitroso-6-hydroxyquinoline derivatives.

Пример 1. Внутрикомплексное соединение железа (11) с 5-нитрозо-6-оксихинолином.Example 1. Intra-complex compound of iron (11) with 5-nitroso-6-hydroxyquinoline.

2 г 5-нитрозо-6-оксихинолина раствор ют при нагревании в 500 мл этанола, добавл ют 6,8 мл уксусной кислоты и 0,85 г безводного ацетата натри , а затем раствор 0,98 г2 g of 5-nitroso-6-hydroxyquinoline is dissolved by heating in 500 ml of ethanol, 6.8 ml of acetic acid and 0.85 g of anhydrous sodium acetate are added, and then a solution of 0.98 g

сульфата железа (II) в 10 мл воды. Реакционн гю массу кип т т па вод ной бане 3 ч, после чего растворитель упаривают до объема 100 мл, выделившийс  осадок отфильтровывают , промывают на воронке эфиром и сушат. Выход целевого продукта 2,15 г (98%) ст. пл. 350°С.iron (II) sulfate in 10 ml of water. The reaction mass is boiled under a water bath for 3 h, after which the solvent is evaporated to a volume of 100 ml, the precipitate is filtered off, washed on a funnel with ether, and dried. The yield of the target product 2.15 g (98%) Art. square 350 ° C.

Ямакс 298 нм, ,66; 700 нм, Ig 8-4,81.Yamax 298 nm,, 66; 700 nm, Ig 8-4.81.

Найдено, %: N 13,65.Found,%: N 13.65.

CsrHjsNeOsNaFe.CsrHjsNeOsNaFe.

Вычислено, %: N 14,05.Calculated,%: N 14.05.

Пример 2. Внутрикомплексное соединение 5-нитрозо-6-оксихинальдина с железом (II).Example 2. Intra-complex compound 5-nitroso-6-hydroxyhaldine with iron (II).

Получено, как описано в примере 1. Выход целевого продукта 98%, т. пл. 350°.Obtained as described in example 1. The yield of the target product is 98%, so pl. 350 °.

Ямакс 298 нм, ,82; .„акс 700 нм, Ig 8 4,39.Yamax 298 nm,, 82; . „Ax 700 nm, Ig 8 4.39.

Найдено, %: N 12,90.Found,%: N 12.90.

CsoHsiNsOeNaFe.CsoHsiNsOeNaFe.

Вычислено, %: N 13,11.Calculated,%: N 13,11.

Сранительную устойчивость предложенных красителей по сравнению с известными иллюстрирует таблица.The comparative stability of the proposed dyes in comparison with the known ones is illustrated in the table.

Прим. и.е: Эгалнзируюда  спэсобнэсгь определенна  по методу, описанному в справочнике „Хими , М., 1971, стр. 27, равна 5 баллам. прэдлагаемых согдинений на полиамидном волокне, „Красители дл  текстильнЭ.Ч промышленности изд. Note and.e: Egalnizirudu spesobnesg determined by the method described in the directory “Chem., M., 1971, p. 27, is equal to 5 points. proposed proposals on polyamide fiber, “Dyes for textilesE.C industry ed.

Claims (1)

1. Патент США № 2891951, кл. 260-146, 1968.1. US Patent No. 2891951, cl. 260-146, 1968.
SU762404035A 1976-09-07 1976-09-07 Complexes of bivalent iron with derivatives of 5-nitroso-6-oxyquinoline as dyes for natural and synthetic polyamide fibres SU617465A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU762404035A SU617465A1 (en) 1976-09-07 1976-09-07 Complexes of bivalent iron with derivatives of 5-nitroso-6-oxyquinoline as dyes for natural and synthetic polyamide fibres

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU762404035A SU617465A1 (en) 1976-09-07 1976-09-07 Complexes of bivalent iron with derivatives of 5-nitroso-6-oxyquinoline as dyes for natural and synthetic polyamide fibres

Publications (1)

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SU617465A1 true SU617465A1 (en) 1978-07-30

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SU762404035A SU617465A1 (en) 1976-09-07 1976-09-07 Complexes of bivalent iron with derivatives of 5-nitroso-6-oxyquinoline as dyes for natural and synthetic polyamide fibres

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