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المبحث الرابع: المساء مع ذکريات الحبيب

المبحث الرابع: المساء مع ذکريات الحبيب

قصيدة (ذات مساء) لنازک الملائكة[1]

ثورۃ من ألمٍ، من ذکریاتِ
خلف نفسي، ملء[2] إحساسي العنیف[3]
وجموحٌ[4] في دمی، في خلجاتي[5]
في ابتساماتي، في قلبي اللھیف[6]

إن أکن أبسم کالطفلِ السعیدِ
فابتساماتي وھم وخداعُ
إن أکن ھادءۃً، بین الورود
ففؤادي في جنونٍ وصراع

أيّ مآساۃٍ[7] تراھا مقلتایا [8] !
أيّ حزنٍ عاصرٍ[9] في نظراتي!
جمدَت فوق شقاءي شفتایا
وانحنت[10] کفّاي تحت الرعشاتِ[11]

لا تسلْني عن خیالاتي ولحني
فالدجی[12] الآن بغیضُ[13] في عیوني
أین أُلقي بصري الباکي وحزني
إن أنا حوّلتُ عن کفّي عیوني؟

أین أرنو[14] ؟ کلّما حوّلت عیني
طالعتني صورۃ الوجہِ اللّھیف (متوق المشتاق)
ذلک الوجہُ الذي ألھب[15] فنّي
بمعاني الشعر والحبّ العنیفِ

أیّھا الغادرُ، لا تنظر إلیّا
قد سئمتُ[16] الأمل المرَّ الکَذوبا
حسبُ أقداري ما تجني[17] علیّا 
وکفی عمريّ حزناً ولھیبا

فیم أبقی الآن حیرَی في مکاني؟
آہ لو أرجع، لو أنسی شقاءي[18]
أدفِنُ الأحزان في صدرِ الأغاني
وأناجي[19] بالأسی صمتَ المَساءِ

لیتنا لا نلتقي، لیت شقاءي
ظلَّ ناراً، ظلَّ شوقاً وسُھاد[20]
یا دموعي، أيّ معنًی للّقاءِ
إن ذَوَی[21] الحبّ وأبلاہُ[22] البعاد 

أیّھا الأقدار، ما تبغینَ منّا؟
فیم قد جئتِ بنا ھذا المکانا؟
آہِ لو لم نکُ یا أقدارُ جئنا
ھا ھُنا، لو لم تقدنا قد...

قرآن کا صیغہ نہی اور عائلی منکرات

Islam has prescribed its orders either demanding some acts or avoiding from the prohibited acts. This research article is about the Islamic prohibitions regarding family matters. No doubt family is the most sacred and sensitive institution of the society and Islam has well established this institution with its orders providing the ethical, spiriyual and legal values to the Muslim Society. Some of these orders are purely family matters and some are family as well as the matters related to the whole society. This research paper is to elaborate the Islamic prohibitions which affect the family as well as the social life of the individuals and it is just to make the society peaceful and obligation and rights onserving society.

Solution-Phase Synthesis of a Combinatorial N, N′- Disubstituted Thiourea Library: Complexation, Characterization and Biological Studies

A chemical library of N, N''-Disubstituted thioureas have been derived from substituted aromatic carboxylic acids and two types of combinatorial strategies have been employed for the construction of chemical library. For high throughput screening of components of the chemical library, solution-phase pool syntheses have been exercised, where each pool consists of four components. All the members of chemical library have also been synthesized by using a parallel mode of solution-phase combinatorial synthesis for the purpose of lead screening/identification, testing, characterization and for assembling of Cu(I), Cu(II) & Pd(II) metal complexes. Copper(I) (1A-19A, 1B-19B, 1C-19C& 1F) and palladium(II) [(1E-14E)] complexes of N, N''-disubstituted thioureas have only been synthesized with some selected thioureas from sub-library-1 and Cu(II) complexes (1D-6D) with isoureas (1-6), prepared from the thioureas derived from benzoic acid. All the thioureas (1a-40a, 1b-40b, 1c-40c, 1d-40d, 1e-40e, 1f-40f & 1g-40g) and complexes have been characterized by elemental analyses, FT-IR, 1 H & 13 C NMR spectroscopy, mass spectrometry and single crystal XRD. The stability of the Cu(I) complexes in the test medium has been confirmed by cyclic voltammetric studies. The products of pool syntheses (pools 1-40) have been characterized by mass spectrometry and GC-MS (gas chromatograph coupled with mass spectrometer) techniques. In all the Cu(I) and Pd(II) complexes, neutral N, N′-disubstituted thiourea ligands have been coordinated to the metal atom through the sulphur atom in a terminal mode except (1F), where the deprotonation of NH group of the thiourea ligand has facilitated the bonding of copper atom through N and S. The isoureas (1-6) show bidentate behavior in Cu(II) complexes having square planar geometry (1D-6D). The thioureas have also been examined for their fungicidal properties and these show significant activity against various fungi strains and low phytotoxicity for the representative monocot plant species. The complexes have been screened for their in vitro cytotoxicity in human cell lines carcinomas A498 (renal), EVSA-T (breast), H226 (lung), IGROV (ovarian), M19 (melanoma-skin), MCF-7 (breast) and WIDR (colon). They show a moderate cytotoxicity against these seven human cancer cell lines in comparison to that of the less active standard chemotherapeutic drugs. Biological screening of the synthesized thioureas and their metal complexes for various targets is in progress.
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