عبداللطیف تپش
عبداللطیف تپش(۱۸۹۵ء ۔۱۹۴۳ئ) لاہور میں پیدا ہوئے۔ منشی فاضل اور بی۔اے کے امتحانات پاس کرنے کے بعد کچھ عرصہ پنجاب ہائی کورٹ میں ملازمت کی۔ پھر گورنمنٹ انٹر کالج پسرور ضلع سیالکوٹ میں علومِ شرقیہ کے استاد مقرر ہوئے۔ پسرور میں ملازمت کے دوران مزید تعلیم کے لیے مطالعے کو جاری رکھا اور ایم ۔اے فارسی کا امتحان ۱عزاز کے ساتھ پاس کیا۔اس امتحان میں تپشؔ یونیورسٹی بھر میں اول رہے ۔ (۴۱۶) تپشؔ کو شعرو شاعری سے حد سے زیادہ دلچسپی تھی۔ ان کے اوقاتِ تدریس بڑے دلکشا اور معلومات افزا ہوتے۔ کالج میں بزمِ ادب کی جان ہوا کرتے تھے۔ گورنمنٹ کالج پسرور میں قیام کے دوران متعدد ادبی مجالس اور مشاعروںکا مقصد طلبا کے ذوق کی نشوونما اور فروغ زبان اُردو تھا۔ جو بدرجہ اتم ہوا اور کئی طالب علم شاعر بن گئے۔ گورنمنٹ کالج پسرور میں ۴ مارچ ۱۹۳۲ء کو ابو الاثر حفیظ جالندھری تشریف لائے تو کالج کے وائس پرنسپل پروفیسر سراج الدین آذر نے کالج سٹاف کا تعارف کراتے ہوئے عبداللطیف تپشؔ کے بارے میں کہا :
یہ شاعر ہی نہیں شاعر گر بھی ہیں۔(۴۱۷)
تپشؔ کا شعر و شاعری کا ذوق جبلی تھا۔ انھیں سر عبدالقادر (مدیر مخزن) جیسی علمی و ادبی شخصیت کی دامادی کا شرف بھی حاصل تھا۔ جس کی وجہ سے آپ کے شعری ذوق کی بہت جلد اصلاح اور ترقی ہو گئی۔ تپش ؔ نے سر عبدالقادر کی علمی صحبتوں سے بصدِ رنگ استفادہ کیا لیکن آپ کی طبیعت نظم کی طرف مائل نہ ہو سکی۔ بلکہ آپ غزل ہی کے شائق و دلدادہ رہے۔ آپ شروع میں بہت پرگو اور مشکل شاعر تھے لیکن کثرتِ مشق سخن سے ان کے کلام میں سادگی و پرکاری آگئی۔ اُن کے کلام ہندوستان کے ممتاز ادبی رسائل و جرائد میں شائع ہوا کر تاتھا۔ (۴۱۸) آپ...
In this universe, if we look at the arrival of a human being, it will open up to us the secret that man did not come in this world suddenly, but he had gone through several worlds before stepping into this universe. The First World is called spiritual world where his soul was present and the argument is that when the soul enters the body of the baby and he starts to move in the womb of the mother, so the question now arises where was that soul before it entered the baby’s body? And where did that soul come from? Where it was and wherever it came from, the name of that universe is Spiritual world. After the spiritual world, there is a second world in the womb of the mother. In this world a man must live for at least nine months. Stop for a minute to see this amazing system of power that a baby remains alive in a moving grave for at least nine months. The object is to say that if a human being has to go through two worlds before coming into the universe, so if a fourth world is accepted after this world, what is the rational prohibition behind it? The life in the fourth world is called the life of Hereafter. If there is any disagreement with this name then let’s another name, but a fourth world still have to believe, because when the soul comes out of body after death, the same question will arise here that where did the soul go? In this article, it is examined that how author of “Tarjuman al-Qur’an” Abul Kalam Azad has proved the reality of life of Hereafter and what kind of arguments have given as an evidence in this tafsir?
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.