{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/111027"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/111027","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"Preparation of the azo dyes; diazobenzene-acetoacet-alpha-naphthylamide; diazo-alpha-naphthylamine-acetoacetanilide and the isomeric meta- and para-nitro derivatives of diazobenzene-acetoacetanilide","abstract":"I. Dyes were prepared by coupling para- and meta- nitroaniline and alpha-naphthylamine with aceto-acetanilide. II. Intermediates were prepared by condensing para- and meta-nitroaniline and alpha-naphthylamine with aceto-acetanilide. III. Dyes were prepared by diazotizing aniline and coupling with the para- and meta-nitro-aceto-acetanilide. To the present writing, our attempts to couple diazotized aniline with aceto-acet-alpha-naphthylamide have failed because of the extreme insoluble character of the intermediate.","abstract_html":"I. Dyes were prepared by coupling para- and meta- nitroaniline and alpha-naphthylamine with aceto-acetanilide. II. Intermediates were prepared by condensing para- and meta-nitroaniline and alpha-naphthylamine with aceto-acetanilide. III. Dyes were prepared by diazotizing aniline and coupling with the para- and meta-nitro-aceto-acetanilide. To the present writing, our attempts to couple diazotized aniline with aceto-acet-alpha-naphthylamide have failed because of the extreme insoluble character of the intermediate.","abstract_has_math":false,"creators":["Russell, Ella G."],"institution":"Virginia Agricultural and Mechanical College and Polytechnic Institute","degree_name":"M.S.","degree_level":"masters","degree_discipline":"Applied Chemistry","degree_department":"Applied Chemistry","school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1928,"date_issued":"1928","date_published":"1928","updated_at":"2026-07-22T22:19:09Z","subjects":[],"languages":["en"],"rights":["In Copyright"],"rights_urls":["http://rightsstatements.org/vocab/InC/1.0/"],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10919/111027","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.department","label":"Department","values":["Applied Chemistry"]},{"key":"dc:creator","label":"Author","values":["Russell, Ella G."]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2022-06-29T19:26:46Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2022-06-29T19:26:46Z"]},{"key":"dc:date.issued","label":"Date","values":["1928"]},{"key":"dc:publisher","label":"Institution","values":["Virginia Agricultural and Mechanical College and Polytechnic Institute"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.dcmitype","label":"Dc Type Dcmitype","values":["Text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Applied Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M.S."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Virginia Agricultural and Mechanical College and Polytechnic Institute"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["In Copyright"]},{"key":"dc:rights.uri","label":"Rights URI","values":["http://rightsstatements.org/vocab/InC/1.0/"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/111027"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["I. Dyes were prepared by coupling para- and meta- nitroaniline and alpha-naphthylamine with aceto-acetanilide. II. Intermediates were prepared by condensing para- and meta-nitroaniline and alpha-naphthylamine with aceto-acetanilide. III. Dyes were prepared by diazotizing aniline and coupling with the para- and meta-nitro-aceto-acetanilide. To the present writing, our attempts to couple diazotized aniline with aceto-acet-alpha-naphthylamide have failed because of the extreme insoluble character of the intermediate."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["M.S."]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Preparation of the azo dyes; diazobenzene-acetoacet-alpha-naphthylamide; diazo-alpha-naphthylamine-acetoacetanilide and the isomeric meta- and para-nitro derivatives of diazobenzene-acetoacetanilide"]}]}],"canonical_facts":{"dc:contributor.department":["Applied Chemistry"],"dc:creator":["Russell, Ella G."],"dc:date.accessioned":["2022-06-29T19:26:46Z"],"dc:date.available":["2022-06-29T19:26:46Z"],"dc:date.issued":["1928"],"dc:description.abstract":["I. Dyes were prepared by coupling para- and meta- nitroaniline and alpha-naphthylamine with aceto-acetanilide. II. Intermediates were prepared by condensing para- and meta-nitroaniline and alpha-naphthylamine with aceto-acetanilide. III. Dyes were prepared by diazotizing aniline and coupling with the para- and meta-nitro-aceto-acetanilide. To the present writing, our attempts to couple diazotized aniline with aceto-acet-alpha-naphthylamide have failed because of the extreme insoluble character of the intermediate."],"dc:description.degree":["M.S."],"dc:format.mimetype":["application/pdf"],"dc:identifier.uri":["http://hdl.handle.net/10919/111027"],"dc:language.iso":["en"],"dc:publisher":["Virginia Agricultural and Mechanical College and Polytechnic Institute"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:title":["Preparation of the azo dyes; diazobenzene-acetoacet-alpha-naphthylamide; diazo-alpha-naphthylamine-acetoacetanilide and the isomeric meta- and para-nitro derivatives of diazobenzene-acetoacetanilide"],"dc:type":["Thesis"],"dc:type.dcmitype":["Text"],"thesis:degree_discipline":["Applied Chemistry"],"thesis:degree_level":["masters"],"thesis:degree_name":["M.S."],"thesis:institution_name":["Virginia Agricultural and Mechanical College and Polytechnic Institute"]},"updated_at":"2026-07-22T22:19:09Z"}