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History of Hindko

Thesis Info

Author

Syeda Sumaira Bukhari

Department

Pakistan Study Centre

Program

MA

Institute

University of Peshawar

Institute Type

Public

City

Peshawar

Country

Pakistan

Degree Starting Year

1989

Degree End Year

1991

Subject

Pak Studies

Language

English

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676710688521

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خوش رنگ و خوش نما ہے وہ گنبد جو سبز ہے

خوش رنگ و خوش نما ہے وُہ گنبد جو سبز ہے
آنکھوں میں بس رہا ہے وُہ گنبد جو سبز ہے

اِس نامۂ سیاہ کے بدلے پنہ کہاں؟
ہاں ایک آسرا ہے وُہ گنبد جو سبز ہے

چہرے پہ جو لکھی ہے وہ زردی ہے خوف کی
آنکھوں میں تیرتا ہے وہ گنبد جو سبز ہے


دل بھی سفید رنگ کبوتر ہے آس کا
یہ بھی تو ڈھونڈتا ہے وُہ گنبد جو سبز ہے

نیلاہٹوں میں غرق ہے مسموم ہے فضا
تریاق بانٹتا ہے وُہ گنبد جو سبز ہے

میرے لہو سے سُرخ ہے عابدؔ یہ راہِ شوق
مجھ کو بُلا رہا ہے وُہ گنبد جو سبز ہے

Conditions and Qualification for Being a Judge in the Light of the Islamic Law

‘Adl and Qisṭ is indeed a manifestation of God’s mercy, rather, it may also be seen as a principal objective of Shariʿah. The origin or sources of administration of justice in Islām are the Quran, Sunnah of the holy Prophet, consensus of opinions of the jurists of Islamic jurisprudence and Analogy (Qiyās). Justice is a sacred obligation of supererogatory. It is obligatory upon the Muslim rulers to appoint judges for the dispensation of justice to attain equality, to protect the human rights from their violation, to safeguard the lives and properties, and to maintain law and order in society. As a judge is supposed to accomplish a very important and noble task being a regent of Allāh, hence, some vital merits and criteria regarding the conditions and qualifications for the appointment of the Qāḍī or judge in the light of the Qur’ān, Sunnah and Islamic jurisprudence and the code of conduct for the Pakistani judges must be observed at all costs. The author of this paper has discussed these conditions and qualifications in this article. There are some unanimous conditions for the appointment of judges, while some others are not agreed upon. While presenting the difference of opinions of the Islamic jurists, the author tried to explain, reconcile the opinions and at some places presented her own view in the light of her analysis and arguments. These conditions are around thirty, but the author according to her own discretion chose some of the most important ones to discuss in this paper.

Synthesis of Ag I -N-Heterocyclic Carbene and Cyclonickellated Complexes for Chemical and Biological Studies

Metal complexes exhibit a wide variety of functional groups in drug designing and development due their vaious chemical properties, coordination modes, geometries and reactivities. Organonikellated and silver complexes have become attractive tool in the field of catalytic as well as medicinal chemistry. The present project was designed to synthesize new series of silver-N-Heterocyclic carbene (NHC) and cyclonickellated complexes. Various NHC based as well as phosphine/phosphinite based precursors were designed leading to the synthesis of target silver and nickel complexes, respectively. Three series (A-C) of novel mono- and bisimidazolium salts (1a-16a, 1b-12b, 1c-7c) as ligands and their mono, di, tri and polynuclear silver complexes (17a-20a, 13b-20b, 8c-12c) were synthesized. The corresponding silver(I) aducts were afforded by the in situ deprotonation of the NHC based ligands. Some of the NHC salts (7a-12a) of series A were found to be difficult to react with silver due to steric factor (bulky alkyl substituents attached to them), so their silver complexes could not be synthesized. The synthetic approaches of the ligands of series B were controlled by the methyl substituents attached to the backbone of benzimidazole imposing significant impact on the reactivity by the virtue of their aptitude to enhance sigma electron donating ability of ligands. The precursors and silver complexes were well characterized by FTIR, GC-MS, 1H, 13C (one and two dimensional), 31P and 19F NMR, elemental analysis, melting points, ESI-MS and single crystal X-ray crystallographic techniques. Adopting a different protocol of synthesis using excess of reactant, an interesting trinuclear silvercomplex (8c) was synthesized. After successful syntheses, the silver complexes were employed to study their redox potentials by cyclic voltammetry. The quasi reversibility and irreversibility of redox events in the electrochemical study of silver complexes indicated that the reduction event produces unstable decomposed species and oxidation event may be ascribed to decomposed species. Azolium salts and their Ag(I)-NHC complexes were tested in vitro against Bacillus subtillis, Macrococcus brunensis, and Bacillus cereus to study their antibacterial activity and against MDA-MB-231 and HCT116 cells to study their anticancer potential. All compounds were observed to pose potential antibacterial and anticancer activity, however, silver-NHC complexes were found relatively more potent compared to the corresponding NHC precursors (salts). Only few salts were found inactive, while their complexes were observed to be active concluding that the silver imparts greater anticancer potential to the compounds. Being air and moisture sensitive, cyclonickellated complexes could not be utilized for evaluation of their antimicrobial, anticancer or redox potential, however, the attempts were made to study their functionalization behaviour under inert atmosphere. It was observed that the coordination of PR2 moiety into CNi bond is apparent from the initial colour change and shift of 31P NMR and 19F NMR signals but final products of insertion remained difficult to be analyzed as they usually decomposed or appeared NMR silent after workup.In order to understand the feasibility of reaction and to evaluate the properties of product of insertion, further attempts were made to get target complexes via different way by synthesizing phosphine-phosphinite ligands and reacting them with nickel precursor. Appearance of specific signals in NMR spectra of few products provided some evidences of formation of the target products but later the products decomposed and signals disappeared. Thus the products of all reactions were very difficult to identify by NMR either due to paramagnetic nature or decomposition of products and crystallization attempts remained unsuccessful so their structures remained ambiguous as no other technique could help to study them due to their air/moisture sensitivity. On the whole the present project provided useful information for drug designing and chemical transformation studies.