{"id":22,"date":"2022-06-04T14:45:00","date_gmt":"2022-06-04T14:45:00","guid":{"rendered":"http:\/\/profstefanberger.de\/?page_id=22"},"modified":"2022-09-29T18:39:54","modified_gmt":"2022-09-29T18:39:54","slug":"publications-1985-1981","status":"publish","type":"page","link":"https:\/\/profstefanberger.de\/?page_id=22","title":{"rendered":"Publications 1985 &#8211; 1981"},"content":{"rendered":"\r\n<h5 style=\"text-align: center;\"><span style=\"color: #000000;\">No. 29 &#8211; 42<\/span><\/h5>\r\n<p style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif;\"><b><span style=\"font-size: 18px;\">Publications 1985<\/span><\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">T. Dave, S. Berger, E. Bilger, H. Kaletsch, J. Pebler, J. Knecht und K. Dimroth, \u201cIron Complexes of Phosphinine Derivatives&#8221;,<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Organometallics <\/i><b>1985, <\/b><i>4, <\/i>1565-1572.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/art1lib.org\/book\/29158346\/9a1c8e\">DOI: 10.1021\/om00128a014<\/a>.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">H. K\u00fcnzer and S. Berger, \u201cStrained Benzene Derivatives by Copper Catalyzed tert.-Butylation&#8221;, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. Org. Chem. <\/i><b>1985, <\/b><i>50, <\/i>3222-3223.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1021\/jo00217a045\">DOI: 10.1021\/jo00217a045<\/a>.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">H. K\u00fcnzer and S. Berger, \u201cSpectroscopic Determination of <sub>I<\/sub>&#8211; and <sub>R<\/sub>-Substituent Constants for the Deuterium Atom&#8221;, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. Am. Chem. Soc. <\/i><b>1985, <\/b><i>107, <\/i>2804-2805.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1021\/ja00295a041\">DOI: 10.1021\/ja00295a041<\/a>.<br \/><br \/><\/span><\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif;\"><b><span style=\"font-size: 18px;\">Publications 1984<\/span><\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">H. K\u00fcnzer and S. Berger, \u201cThe Deuterium Isotope as a Polar Substituent?\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Tetrahedron Letters <\/i><b>1984, <\/b><i>25, <\/i>5019-5022.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1016\/S0040-4039(01)91107-4\">DOI: 10.1016\/S0040-4039(01)91107-4<\/a>.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, \u201c<sup>13<\/sup>C,<sup>13<\/sup>C Spin-Spin Coupling Constants as a Probe for Mesomeric Structures &#8211; Vitamin C\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. C. S. Chem. Comm. <\/i><b>1984,<\/b> 1252-1253.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"http:\/\/www.rsc.org\/Publishing\/Journals\/C3\/article.asp?doi=C39840001252\">DOI: 10.1039\/C39840001252<\/a>.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger and K. P. Zeller, \u201cA <sup>13<\/sup>C,<sup>13<\/sup>C Spin, Spin Coupling Matrix for Azulene\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. Org. Chem<\/i>. <b>1984, <\/b><i>49, <\/i>3725-3728.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/ur.booksc.eu\/book\/28990025\/be338b\">DOI: 10.1021\/jo00194a011.<\/a><br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, \u201cA <sup>13<\/sup>C,<sup>13<\/sup>C Spin, Spin Coupling Matrix for 1- and 2-Methylnaphthalene by the Two-Dimensional INADEQUATE Method. Correlation with -bond Orders\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Org. Magn. Res. <\/i><b>1984, <\/b><i>22, <\/i>47-51.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1002\/mrc.1270220110\">DOI: 10.1002\/mrc.1270220110<\/a>.<br \/><br \/><\/span><\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif;\"><b><span style=\"font-size: 18px;\">Publications 1983<\/span><\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger and H. K\u00fcnzer, \u201cExtrem weitreichende 2H-Isotopeneffekte auf die chemischen Verschiebungen in <sup>13<\/sup>C-NMR-Spektren von Verbindungen mit konjugierten Doppelbindungen\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Angewandte Chemie <\/i><b>1983, <\/b><i>95,<\/i> 321-322; Int. Ed. <b>1983, <\/b><i>22, <\/i>321-322.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\" https:\/\/www.doi.org\/10.1002\/ange.19830950413\">DOI: 10.1002\/ange.19830950413<\/a>, DOI: 10.1002\/anie.198303212.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger and H. K\u00fcnzer, \u201cLong Range Secondary 2H-Isotope Effects in the <sup>13<\/sup>C-NMR Spectra of Naphthalene and Azulene\u201d,<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Tetrahedron <\/i><b>1983, <\/b><i>39, <\/i>1327-1329.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif;\"><a href=\"https:\/\/www.doi.org\/10.1016\/S0040-4020(01)91900-3\"><span style=\"font-size: 14pt;\">DOI 10.1016\/S0040-4020(01)91900-3<\/span><\/a>.<br \/><br \/><\/span><\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif;\"><b><span style=\"font-size: 18px;\">Publications 1982<\/span><\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">A. Rieker, S. Berger, D. Mootz, M. Steffen and H. Wunderlich \u201cDehydratisierungsprodukte von 2.5-Cyclohexadien-1.4-diolen; <i>die Kristallstruktur von 3.7-Di-tert-butyl-5-phenyl-2-(p-tolyl)-oxepin\u201d, <br \/>Chem. Ber. <\/i><b>1982, <\/b><i>115, <\/i>385-389.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1002\/cber.19821150134\">DOI: 10.1002\/cber.19821150134<\/a>.<br \/><br \/><\/span><\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif;\"><b><span style=\"font-size: 18px;\">Publications 1981<\/span><\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">K. Dimroth, S. Berger, H. Kaletsch \u201cSind <sup>5-<\/sup>Phosphorine cyclische Phosphonium-Ylide oder 6&#8211;delokalisierte \u201daromatische\u201d Verbindungen?\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Phosphorus and Sulfur <\/i><b>1981,<\/b><i>1 0, <\/i>305-316.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1080\/03086648108077381\">DOI: 10.1080\/03086648108077381<\/a>.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">K. Dimroth, S. Berger, H. Kaletsch \u201cDie Phosphonium-Ylidstruktur der Tricarbonylchromkomplexe von <sup>5<\/sup>-Phosphorinen&#8221;,<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Phosphorus and Sulfur <\/i><b>1981, <\/b><i>10, <\/i>295-304.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1080\/03086648108077380&quot;\">DOI: 10.1080\/03086648108077380<\/a>.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">K. P. Zeller and S. Berger, \u201cDarstellung und spektroskopische Charakterisierung von (4.7-<sup>13<\/sup>C<sub>2<\/sub>)-Azulen\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Z. Naturfoschung <\/i><b>1981, 36b<\/b>, 858-864.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1515\/znb-1981-0715\">DOI: 10.1515\/znb-1981-0715<\/a>.<br \/><br \/><\/span><\/li>\r\n<li style=\"text-align: justify;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger \u201cThe pH Dependence of Phenolphthalein\u201d, <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Tetrahedron <\/i><b>1981, <\/b><i>37, <\/i>1607-1611. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif;\"><a href=\"https:\/\/www.doi.org\/10.1016\/S0040-4020(01)92103-9\"><span style=\"font-size: 14pt;\">DOI: 10.1016\/S0040-4020(01)92103-9<\/span><\/a>.<\/span><\/li>\r\n<\/ul>\r\n","protected":false},"excerpt":{"rendered":"<p>No. 29 &#8211; 42 Publications 1985 T. Dave, S. Berger, E. Bilger, H. Kaletsch, J. Pebler, J. Knecht und K. Dimroth, \u201cIron Complexes of Phosphinine Derivatives&#8221;,Organometallics 1985, 4, 1565-1572.DOI: 10.1021\/om00128a014. H. K\u00fcnzer and S. Berger, \u201cStrained Benzene Derivatives by Copper Catalyzed tert.-Butylation&#8221;, J. Org. Chem. 1985, 50, 3222-3223.DOI: 10.1021\/jo00217a045. H. K\u00fcnzer and S. Berger, \u201cSpectroscopic [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":10,"menu_order":2,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-22","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/22","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=22"}],"version-history":[{"count":35,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/22\/revisions"}],"predecessor-version":[{"id":667,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/22\/revisions\/667"}],"up":[{"embeddable":true,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/10"}],"wp:attachment":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=22"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}