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عبدالحلیم شررؔ لکھنوی

مولانا شررؒ
عین اس وقت جب ہم اردو رسالوں کی تاریخ پر ایک سرسری نظر ڈال رہے ہیں، اردو کا وہ سب سے پرانا رسالہ اور اس کا وہ اڈیٹر یاد آتا ہے جس نے سال کے آخری مہینہ کی آخری تاریخوں میں ہماری دنیا کو الوداع کہا، یعنی مولانا عبدالحلیمؔ شرر صاحب لکھنوی، اڈیٹر دل گداز، مولانا ہمارے انشاء پردازوں میں سب سے پرانے انشاء پرداز تھے، اکہتر (۷۱) برس کی عمر میں بعارضۂ فالج وفات پائی، مرحوم نے اپنی عزت اور شہرت تنہا خود اپنے قلم سے حاصل کی تھی، وہ اپنی شہرت کے لئے کسی نامور ہستی سے انتساب کے ممنون نہ تھے، انہوں نے اپنے تمام معاصرین میں سب سے زیادہ اپنی زبان کی خدمت کی فرصت پائی، ہمارے خیال میں ۱۸۸۲؁ء سے انہوں نے اپنے کام کا آغاز کیا اور جو اخیر زمانۂ وفات دسمبر ۱۹۲۶؁ء تک قائم رہا، بیچ بیچ میں کبھی کبھی حیدرآباد کے قیام کی مصروفیتیں پیش آجاتی تھیں، تاہم ان کا تسلسل کبھی ٹوٹنے نہیں پایا، ۴۶ برس کا عہد خدمت ان کے کسی معاصر کو میسر نہیں آیا، پھر ان کی ادبی اور علمی خدمات کی گوناگونی اور کثرت بھی ان کا خاص امتیاز ہے اور یہ کہنا بھی سچ ہے کہ انہیں کی تصنیفات نے اردو میں سینکڑوں انشاء پرداز پیدا کئے اور ملک میں تاریخ کا مذاق پیدا کیا اور سنجیدہ تصنیفات کے لئے حسن قبول کا راستہ صاف کیا۔
خاکسار کو مولانا کا پہلا شرف نیاز ۱۹۰۴؁ء میں حاصل ہوا اور یاد آتا ہے کہ وہ اس وقت حیدرآباد سے واپس آئے تھے اور اتحاد اور پردۂ عصمت نکالنا شروع کیا تھا، وہ عربی زبان کے مستند عالم تھے، بچپن میں وہ اپنے نانا کے ساتھ واجد علی شاہ کے مٹیابرج میں رہے تھے اور اس طرح جب ہوش سنبھالا، تو اپنے کو سخنورانِ اردو...

Running Musharakah Product of Islamic Banks: An Alternative of Running Finance

Islamic banking system is growing day by day. The new era of Islamic banking is very successful as new products are being introduced by Islamic banks to cater the demands of customer under Shariah guidelines, there was demand of a product for working capital as an alternative to the conventional product of running finance. Running Musharakah Product has been introduced as substitute to Running Finance Product. In this paper the concept of Running Finance as well as Running Musharakah is described, the practical steps of running Musharakah are also illustrated to examine the viability of the product.

Synthesis, Characterization and Pharmacological Evaluation of Some 1, 2, 4-Triazole, 1, 3, 4-Oxadiazole, Triazolothiadiazole and Indolinone Derivatives

The work presented in the thesis consists of the synthesis, characterization and pharmacological evaluation of nitrogen-containing heterocyclic compounds. For convenience, the research work presented in this thesis has been divided into four chapters. The first chapter includes, the synthesis, characterization and pharmacological evaluation of 4,5- disubstituted-1,2,4-triazole-3-thiones and 4,5-disubstituted-1,2,4-triazole-3-ones. Both of these target compounds were synthesized by four-step syntheses involving a series of reactions, including esterification of substituted aromatic acids, hydrazide formation and their condensation with substituted isothiocyanates and substituted isocyanates resulting in the formation of thiosemicarbazides and semicarbazides. The former were obtained by refluxing thiosemicarbazides in sodium hydroxide solution (4N) and the latter were formed by refluxing semicarbazides in sodium hydroxide solution (2N). The final products were obtained by neutralizing the reaction mixtures with dilute hydrochloric acid solution. Later on, the synthesized compounds were screened for their antifungal, anti-inflammatory, acetylcholinesterase, alkaline phosphatase and -glucoronidase activities. The second chapter includes the synthesis, characterization and pharmacological evaluation of 1,3,4-oxadiazoles. These compounds were synthesized by refluxing aromatic acid hydrazides with carbon disulfide in ethanolic potassium hydroxide. All of these compounds were checked for their cytotoxic activities using three different cell lines. The third chapter includes the synthesis, characterization and pharmacological evaluation of triazolothiadiazoles-substituted bridged heterocycles. The synthesis involves the formation of 5- substituted-4-amino-1,2,4-triazole-3-thiones by stirring different aromatic hydrazides with carbon disulfide in methanolic potassium hydroxide and resulted in the formation of potassium dithiocarbazinate salts, which on refluxing with hydrazine hydrate, yielded 5-substituted-4- amino-1,2,4-triazoles-3-thiones. Triazolothiadiazoles were formed by refluxing different aromatic acids with 5-substituted-4-amino-1,2,4-triazoles-3-thiones in phosphoryl chloride. All the synthesized compounds were screened for antibacterial, acetylcholinesterase and alkaline phosphatase activities. The fourth chapter addresses the synthesis, characterization and pharmacological evaluation of Schiff bases of isatin, which are known as indolinone derivatives. These compounds were synthesized by the reaction of acid hydrazides with substituted isatins in ethanol. The synthesized compounds were screened for cytotoxic activity.
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