LEADER 02851nam 2200589Ia 450 001 9910455739103321 005 20200520144314.0 010 $a1-280-47109-3 010 $a0-19-535343-9 010 $a0-585-30895-0 035 $a(CKB)111004366529132 035 $a(EBL)431107 035 $a(OCoLC)609831897 035 $a(SSID)ssj0000146494 035 $a(PQKBManifestationID)11150017 035 $a(PQKBTitleCode)TC0000146494 035 $a(PQKBWorkID)10186482 035 $a(PQKB)11615324 035 $a(MiAaPQ)EBC431107 035 $a(Au-PeEL)EBL431107 035 $a(CaPaEBR)ebr10279054 035 $a(CaONFJC)MIL47109 035 $a(EXLCZ)99111004366529132 100 $a19970310d1998 uy 0 101 0 $aeng 135 $aurcn||||||||| 181 $ctxt 182 $cc 183 $acr 200 10$aEncounters with God$b[electronic resource] $ean approach to the theology of Jonathan Edwards /$fMichael J. McClymond 210 $aNew York $cOxford University Press$d1998 215 $a1 online resource (207 p.) 225 1 $aReligion in America series 300 $aDescription based upon print version of record. 311 $a0-19-511822-7 320 $aIncludes bibliographical references (p. 161-176) and index. 327 $aContents; List of Abbreviations; INTRODUCTION: Edwards as an ""Artful Theologian""; 1. APPREHENSION: Spiritual Perception in Jonathan Edwards; 2. SPECULATION: The Theocentric Metaphysics of The Mind; 3. CONTEMPLATION: The Spirituality of the Personal Narrative and Diary; 4. VALUATION: Ethics and Divinity in End of Creation; 5. NARRATION: Drama and Discernment in History of Redemption; 6. PERSUASION: Edwards as a Christian Apologist; CONCLUSION: The Religious Outlook in Edwards; Notes; Bibliography; Index 330 $aThis book offers a broad-based study of Jonathan Edwards as a religious thinker. Much attention has been given to Edwards in relation to his Puritan and Calvinist forebears. McClymond, however, examines Edwards in relation to his eighteenth-century intellectual context. In each of six chapters, he contextualizes and interprets some text or issue in Edwards within the emergent post-Lockean, post-Newtonian culture of the English-speaking world of the 1700's. Among the topics considered are spiritual perception, metaphysics, contemplation, ethics and morality, and apologetics. 410 0$aReligion in America series (Oxford University Press) 606 $aTheology$vEarly works to 1800 608 $aElectronic books. 615 0$aTheology 676 $a230.58092 676 $a230/.58/092 700 $aMcClymond$b Michael James$f1958-$0886267 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910455739103321 996 $aEncounters with God$91978923 997 $aUNINA LEADER 05148nam 2200613 450 001 996202137103316 005 20230421044620.0 010 $a1-281-84274-5 010 $a9786611842741 010 $a3-527-61527-X 010 $a3-527-61526-1 035 $a(CKB)1000000000376623 035 $a(EBL)481589 035 $a(OCoLC)289271507 035 $a(SSID)ssj0000204196 035 $a(PQKBManifestationID)11184611 035 $a(PQKBTitleCode)TC0000204196 035 $a(PQKBWorkID)10187770 035 $a(PQKB)10365838 035 $a(MiAaPQ)EBC481589 035 $a(EXLCZ)991000000000376623 100 $a20160818h19951995 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aModern acetylene chemistry /$fedited by P. J. Stang and F. Diederich 210 1$aWeinheim, [Germany] :$cVCH,$d1995. 210 4$dİ1995 215 $a1 online resource (530 p.) 300 $aDescription based upon print version of record. 311 $a3-527-29084-2 320 $aIncludes bibliographical references at the end of each chapters and index. 327 $aModern Acetylene Chemistry; Contents; Foreword; List of Contributors; 1 Modern Computational and Theoretical Aspects of Acetylene Chemist; 1.1 Introduction; 1.2 Electronic structures of acetylene and monoacetylenes; 1.2.1 Ground-state potential energy surfaces; 1.2.2 Excited-state potential energy surfaces; 1.2.3 Radical Ions; 1.3 Reactivities and molecular interactions of acetylenes; 1.3.1 Pericyclic reactions; 1.3.2 Electrophilic reactions; 1.3.3 Nucleophilic additions; 1.3.4 Radical additions; 1.3.5 Molecular complexes; 1.4 Polyacetylenes; 1.4.1 Diacetylene; 1.4.2 Cn and cyclic Cn 327 $a1.4.2.1 C21.4.2.2 C3; 1.4.2.3 C4; 1.4.2.4 C5, C7, and C9; 1.4.2.5 C6, C8 and C10; 1.4.2.6 C11 to C17; 1.4.2.7 C18; 1.5 Conclusion; References; 2 Functionalized Acetylenes in Organic Synthesis - The Case of the 1-Cyano- and the 1-Halogenoacetylenes; 2.1 Introduction; 2.2 Synthesis and preparative use of cyanoacetylenes; 2.2.1 Synthesis; 2.2.2 Preparative use of cyanoacetylenes; 2.2.2.1 A short summary of the older literature; 2.2.2.2 Novel cycloadditions with cyanoacetylenes - simple and efficient methods for the construction of complex carbon frame 327 $a2.2.2.3 Cyanoacetylenes as precursors for reactive and interstellar intermediates2.3 Synthesis and preparative use of 1-halogenoacetylenes; 2.3.1 Older review of the literature on halogenoacetylenes; 2.3.2 Synthesis of 1-halogenoacetylenes; 2.3.2.1 The preparation of the 1-Halogeno- and 1,2-Dihalogenoethynes; 2.3.2.2 More highly unsaturated halogenoacetylenes; 2.3.2.3 Derivatives of 1-halogenoacetylenes; 2.3.3 Novel preparative uses of 1-Halogeno- and 1,2-Dihalogenoacetylenes; 2.4 Experimental procedures; 2.4.1 Cyanoacetylene (1); 2.4.2 Dicyanoacetylene (2); 2.4.3 Dicyanodiacetylene (3) 327 $a2.4.4 Chloroacetylene (93)2.4.5 Dichloroacetylene (100); 2.4.6 Diiodoacetylene (105); References; 3 Alkynyliodonium Salts: Electrophilic Acetylene Equivalents; 3.1 Introduction; 3.2 Preparation and properties; 3.2.1 Alkynyliodonium sulfonates; 3.2.2 Alkynyliodonium tetrafluoroborates; 3.2.3 Heterocyclic alkynyliodonium species; 3.2.4 Mechanism of formation; 3.2.5 Diynyliodonium and dialkynyliodonium triflates; 3.2.6 Bis-iodonium species; 3.2.7 Properties of alkynyliodonium salts; 3.3 Characterization and structure; 3.3.1 Spectroscopic properties; 3.3.2 X-ray and molecular structure 327 $a3.4 Reactions and uses of alkynyliodonium salts3.4.1 Reaction with nucleophiles; 3.4.1.1 Carbon nucleophiles; 3.4.1.2 Nitrogen nucleophiles; 3.4.1.3 Oxygen nucleophiles; 3.4.1.4 Sulfur nucleophiles; 3.4.1.5 Phosphorus nucleophiles; 3.4.1.6 Halogen nucleophiles; 3.4.2 Reaction with organometallic species; 3.4.3 Cycloaddition reactions; 3.4.3.1 [2 + 4]-Diels-Alder cycloadditions; 3.4.3.2 1,3-Dipolar cycloadditions; 3.5 Conclusions; 3.6 Experimental procedures; 3.6.1 (Cyano{[(trifluoromethyl)sulfonyl]oxy)iodo}benzene, 7 327 $a3.6.2 General procedure for the preparation of ?-alkyl- and ?-phenylethynyl(phenyl)iodonium triflates, 10 330 $aThis comprehensive handbook presents the full potential of modern acetylene chemistry, from organic synthesis through materials science to bioorganic chemistry.K. Houk, H. Hopf, P. Stang, K. M. Nicholas, N. Schore, M. Regitz, K. C. Nicolaou, R. Gleiter, L. Scott, R. Grubbs, H. Iwamura, J. Moore, and F. Diederich - internationally renowned authors introduce the reader, in a didactically skilful manner, to the state-of-the-art in alkyne chemistry. Emphasis is placed on presenting carefully selected and instructive examples as well as essential references to the original literature.