شاہ عزالدین پھلواروی ندوی
شاہ عزالدین پھلواروی علمی اور دینی حلقوں کے لئے محتاج تعارف نہیں، اپنے مواعظ اور تصانیف کی وجہ سے خاصے معروف ہیں، ابھی چند ہی مہینہ کی تو بات ہے جب انھیں عربی زبان اور اسلامی علوم میں مہارت کی بناء پر حکومت ہند نے اعزاز عطا کیا تھا، اور معارف نے اس سلسلہ میں انھیں مبارکباد دی تھی، کسے معلوم تھا کہ وہ اتنی جلد اس دنیا سے رخصت ہوجائیں گے۔
ادھر کچھ عرصہ سے ان کی صحت مضمحل رہنے لگی تھی، اس لئے انھوں نے سفر ترک کردیئے تھے، لیکن پورنیہ کے کچھ لوگ ان کے بے حد معتقد تھے، ان کی آرزو تھی کہ وہ اپنی تشریف آوری سے انھیں عزت بخشیں اور انھیں اپنے مواعظ سے مستفید فرمائیں، شاہ صاحب نے ناسازی مزاج کا عذر کیا، مگر جب معتقدین کا اصرار جاری رہا تو آمادہ ہوگئے تاکہ ان کے دلوں کو ٹھیس نہ پہنچے، مومن کے دل کو خوش کرنا بڑے ثواب کا باعث ہے، انھیں اس سلسلہ میں آقائے دو جہاںﷺ کی ہدایات یاد تھیں، اس لئے اپنی تکلیف کو نظرانداز کرکے آمادہ سفر ہوگئے، راستہ بخیر گزرا، پورنیہ پہونچ کر بھی ایک آدھ دن طبیعت ٹھیک رہی لیکن پھر ضعف کے ساتھ درد سینہ کی شکایت محسوس ہوتی، جو برابر بڑھتی رہی، جب مقامی دوا دارو سے طبیعت قابو میں نہ آئی، تو لوگ کسی بڑے ڈاکٹر کو بلانے کے لئے شہر گئے، مگر ساری تگ و دو بے کار ثابت ہوئی اور بالآخر وطن سے دور عزیزوں سے مہجوری کے عالم میں جان جان آفریں کے سپرد کردی، نعش پھلواری لائی گئی اور خاندانی قبرستان میں سپردخاک کئے گئے، وہ مجھ سے عمر میں چند سال بڑے تھے، تعلیم میں بھی دو تین درجے آگے تھے، لیکن طلبائے ندوہ کی انجمن الاصلاح میں میرا ان...
Despite the greenness of youth, it is a moment in a Muslim's life when his belief is likely to be hardened frequently by enticements and temptations. It is the responsibility of young Muslims to triumph over these enticements and protect their Islamic way of life, obey the teachings of Prophet, share Islam with others and study the teachings of the Holy Qur’ān. After the fulfillment of these essential obligations, young Muslims are predictable above all to play a significant role in reformation of society. Within the Muslim circle, it is supposed that youth is the most imperative period of life. Youth as bone of nation plays a vital role. They have the capacity to build nation of towards success in all the fields of life by utilizing the abilities. This is the time in which opinions, habits and beliefs are formed, and it is vital for the time to be spent in individual development. For instance, Muslim youth should dedicate themselves into making and spreading the glimpses of Sīrah in society; by avoiding the temptations of time in loneliners and solitude andwith the opposite sex and of seeking knowledge by following the preaching’s of Prophet Muhammad (r). In this way, Muslim youth will be a spiritually strong enough to serve as a role model for other young people and society as whole. The article manifests the same components in the light of teachings of Holy prophet (r). Consolidating with Qur'anic verses, imminent exegetical literature and sayings of the companions of Prophet Muhammad (r), youth can play an active and positive role in reformation and development of society.
In this study, ten new series of triorganotin(IV) derivatives of carboxylates have been synthesized in a result of reaction between tri-organotin(IV) chlorides or tri-organotin(IV) hydroxides with carboxylate ligands of highly active and renound medicines of famous family of quinolones, flouro quinolones and few other such drugs in dry toluene. The ligands (HL1-HL10) used themselves very famous for their activities against most of the bacterial and fungal strains. The mode of coordination of these ligands, structural confirmation and geometric assignments of all the synthesized complexes (1-60) both in solid and liquid states were checked, using various analytical techniques in combination such as FT-IR, multinuclear (1H, 13C and 119Sn) NMR, CHNS analysis, mass spectrometry, TGA-DSCand single crystal X-ray analysis. On the basis of these results, most of the ligands appeared to coordinate to Sn atom through carboxylate moiety except thiobenzoic acid due to the formation of dimer. The trimethyltin (IV) and tributyltin(IV) derivatives posses trigonal bipyramidal geometry both in solid and solution state while triphenyltin(IV) have shown tetrahedral geometry specially due to bulky nature of phenyl groups. The binding/interaction of newly synthesized compounds with SS-DNA was checked by UV-visible Spectroscopic technique and on the basis of viscosity measurement method in the presence and absence of complexes. A hypochromic effect along with obvious bathochromic shift (red shift) was seen in UV studies. These are the clear indications of intercalation mode of interaction. The complex-DNA adduct was formed with great spontaneity as does indicated by the negative values of ∆G for all the evaluated complexes. These results were also well supported by complex-DNA intercalation when checked by viscosity measurement method. All of the newly synthesized complexes were also checked in terms of their antibacterial and antifungal behaviour against several different medically important bacterial and fungal strains whose culture were already prepared and was taken from market. All of the new triorganotin (IV) derivatives have shown significant antibacterial and antifungal activities, more than their respective ligands. Furthermore, most of the newly synthesized compounds were found to have fair antimicrobial activities comparable to the reference drugs. These observations gave the idea that most of these compounds may potentially be used as effective antibacterial and antifungal agents in the coming future. The antitumor and anticancer behaviour of the representative complexes were very positive especially when antitumor agent not only could serve for the treatment of tumors but also can act as a potential source of chemo protective agent which was the worst challenge for all the chemists who are presently working in the field of medicinal synthesis. The leishmaniocidal activities of few of the synthesized compounds were also evaluated and it was found that some of the compounds have shown strong antileishmanial activities. Therefore, the results demonstrated that these synthesized complexes can potentially be used as a new source of novel agents for the effective treatment of leishmaniasis.