[ { "key": "AU3DB8V7", "version": 21, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/AU3DB8V7", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/AU3DB8V7", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/AQVBDSUS", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "AU3DB8V7", "version": 21, "parentItem": "AQVBDSUS", "itemType": "attachment", "linkMode": "linked_url", "title": "Google Patents PDF", "accessDate": "2015-08-25T23:07:36Z", "url": "http://patentimages.storage.googleapis.com/pdfs/US4015995.pdf", "note": "", "contentType": "application/pdf", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:07:36Z", "dateModified": "2015-08-25T23:07:36Z" } }, { "key": "AQVBDSUS", "version": 21, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/AQVBDSUS", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/AQVBDSUS", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Hess", "parsedDate": "1977-04-05", "numChildren": 1 }, "data": { "key": "AQVBDSUS", "version": 21, "itemType": "patent", "title": "Method for delaying the setting of an acid-settable liquid in a terrestrial zone", "creators": [ { "creatorType": "inventor", "firstName": "Patrick H.", "lastName": "Hess" } ], "abstractNote": "In an improved method for the treatment of a permeable formation or zone adjacent to the bore of an oil well, the setting time of an acid-settable liquid is predictably delayed by use of a novel catalyst system. The method provides an effective means for controlling the reduction of the permeability of the formation or zone in a single stage treatment by dissolving the catalyst in the liquid and introducing the solution into the formation. The catalyst system comprises a mixture of a suitable acid-releasing compound and a base.", "place": "", "country": "United States", "assignee": "Chevron Research Company", "issuingAuthority": "", "patentNumber": "US4015995 A", "filingDate": "Aug 25, 1975", "pages": "", "applicationNumber": "", "priorityNumbers": "", "issueDate": "Apr 5, 1977", "priorityDate": "", "references": "", "legalStatus": "", "DOI": "", "citationKey": "", "url": "http://www.google.com/patents/US4015995", "accessDate": "2015-08-25T23:07:36Z", "shortTitle": "", "language": "", "rights": "", "extra": "U.S. Classification 106/287.28, 106/900, 166/295, 106/287.3, 106/287.32; International Classification C08G65/36, C09K8/50, C09K8/60; Cooperative Classification C09K8/50, C08G65/36, C09K8/60, Y10S106/90; European Classification C09K8/60, C09K8/50, C08G65/36", "tags": [], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:07:36Z", "dateModified": "2015-08-25T23:07:36Z" } }, { "key": "MC24WNRG", "version": 20, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/MC24WNRG", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/MC24WNRG", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Alonso et al.", "parsedDate": "2013", "numChildren": 0 }, "data": { "key": "MC24WNRG", "version": 20, "itemType": "journalArticle", "title": "Integrated conversion of hemicellulose and cellulose from lignocellulosic biomass", "creators": [ { "creatorType": "author", "firstName": "David Martin", "lastName": "Alonso" }, { "creatorType": "author", "firstName": "Stephanie G.", "lastName": "Wettstein" }, { "creatorType": "author", "firstName": "Max A.", "lastName": "Mellmer" }, { "creatorType": "author", "firstName": "Elif I.", "lastName": "Gurbuz" }, { "creatorType": "author", "firstName": "James A.", "lastName": "Dumesic" } ], "abstractNote": "", "publicationTitle": "Energy Environ. Sci.", "publisher": "", "place": "", "date": "2013", "volume": "6", "issue": "1", "section": "", "partNumber": "", "partTitle": "", "pages": "76-80", "series": "", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "", "DOI": "10.1039/C2EE23617F", "citationKey": "", "url": "http://xlink.rsc.org/?DOI=C2EE23617F", "accessDate": "2015-08-25T23:07:09Z", "PMID": "", "PMCID": "", "ISSN": "1754-5692, 1754-5706", "archive": "", "archiveLocation": "", "shortTitle": "", "language": "en", "libraryCatalog": "CrossRef", "callNumber": "", "rights": "", "extra": "", "tags": [], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:07:09Z", "dateModified": "2015-08-25T23:07:09Z" } }, { "key": "3GJH8THD", "version": 19, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/3GJH8THD", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/3GJH8THD", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/32N8GXZ6", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "3GJH8THD", "version": 19, "parentItem": "32N8GXZ6", "itemType": "attachment", "linkMode": "linked_url", "title": "Google Patents PDF", "accessDate": "2015-08-25T23:06:23Z", "url": "http://patentimages.storage.googleapis.com/pdfs/US4791022.pdf", "note": "", "contentType": "application/pdf", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:06:23Z", "dateModified": "2015-08-25T23:06:23Z" } }, { "key": "T9CZ26HS", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/T9CZ26HS", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/T9CZ26HS", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/6EPQBFPH", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "T9CZ26HS", "version": 18, "parentItem": "6EPQBFPH", "itemType": "attachment", "linkMode": "linked_url", "title": "ACS Full Text PDF w/ Links", "accessDate": "2015-08-25T23:04:31Z", "url": "http://pubs.acs.org/doi/pdfplus/10.1021/jf970657c", "note": "", "contentType": "application/pdf", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:04:31Z", "dateModified": "2015-08-25T23:04:31Z" } }, { "key": "6EPQBFPH", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/6EPQBFPH", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/6EPQBFPH", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Tressl et al.", "parsedDate": "1998-01-01", "numChildren": 2 }, "data": { "key": "6EPQBFPH", "version": 18, "itemType": "journalArticle", "title": "New Melanoidin-like Maillard Polymers from 2-Deoxypentoses", "creators": [ { "creatorType": "author", "firstName": "Roland", "lastName": "Tressl" }, { "creatorType": "author", "firstName": "Georg T.", "lastName": "Wondrak" }, { "creatorType": "author", "firstName": "Ralph-Peter", "lastName": "Krüger" }, { "creatorType": "author", "firstName": "Dieter", "lastName": "Rewicki" } ], "abstractNote": "In the 2-deoxy-d-ribose/methyl 4-aminobutyrate Maillard system a trapped N-substituted 2-(hydroxymethyl)pyrrole is one of the major products. However, nontrapped representatives of this type of compound were hitherto not found in other Maillard model systems, indicating their extraordinary reactivity. Model experiments with 2-deoxy-d-ribose/methylamine enabled the detection of N-methyl-2-(hydroxymethyl)pyrrole (1) and some derived linear oligomers (2, 3) as minor components. Consequently, 1 was synthesized and its oligomerization studied under very mild acidic conditions. The deformylated dimeric bis(N-methyl-2-pyrrolyl)methane (2) and trimeric N-methyl-2,5-bis(N-methyl-2-pyrrolylmethyl)pyrrole (3) were characterized by GC/MS and NMR. Higher regular oligomers up to 6 N-methyl-2-pyrrolylmethyl units as well as corresponding dehydro-oligomers up to 12 units were identified by MALDI-TOF-MS. A complementary experiment starting with N-methyl-2-hydroxy[13C]methylpyrrole ([13CH2OH]-1) confirmed the structure and the oligomerization pathway. The possible significance of this type of model oligomer for the melanoidin formation in Maillard reactions is discussed. The antioxidative activity of the isolated dimer and trimer was tested in Fe(III)?thiocyanate and DPPH assays. Keywords: Maillard system 2-deoxy-d-ribose/methylamine; oligomerization of N-methyl-2-hydroxymethyl(and hydroxy[13C]methyl)pyrrole; antioxidative activity; model compounds for melanoidins", "publicationTitle": "Journal of Agricultural and Food Chemistry", "publisher": "", "place": "", "date": "January 1, 1998", "volume": "46", "issue": "1", "section": "", "partNumber": "", "partTitle": "", "pages": "104-110", "series": "", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "J. Agric. Food Chem.", "DOI": "10.1021/jf970657c", "citationKey": "", "url": "http://dx.doi.org/10.1021/jf970657c", "accessDate": "2015-08-25T23:04:31Z", "PMID": "", "PMCID": "", "ISSN": "0021-8561", "archive": "", "archiveLocation": "", "shortTitle": "", "language": "", "libraryCatalog": "ACS Publications", "callNumber": "", "rights": "", "extra": "", "tags": [], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:04:31Z", "dateModified": "2015-08-25T23:04:31Z" } }, { "key": "3NPGRI2R", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/3NPGRI2R", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/3NPGRI2R", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/6EPQBFPH", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "3NPGRI2R", "version": 18, "parentItem": "6EPQBFPH", "itemType": "attachment", "linkMode": "linked_url", "title": "ACS Full Text Snapshot", "accessDate": "2015-08-25T23:04:31Z", "url": "http://pubs.acs.org/doi/full/10.1021/jf970657c", "note": "", "contentType": "text/html", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:04:31Z", "dateModified": "2015-08-25T23:04:31Z" } }, { "key": "RKXIBDVS", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/RKXIBDVS", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/RKXIBDVS", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/I3J525JN", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "RKXIBDVS", "version": 18, "parentItem": "I3J525JN", "itemType": "attachment", "linkMode": "linked_url", "title": "ScienceDirect Snapshot", "accessDate": "2015-08-25T23:04:21Z", "url": "http://www.sciencedirect.com/science/article/pii/S0379677998008224", "note": "", "contentType": "text/html", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:04:21Z", "dateModified": "2015-08-25T23:04:21Z" } }, { "key": "I3J525JN", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/I3J525JN", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/I3J525JN", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Batista and de Souza", "parsedDate": "1999-05", "numChildren": 2 }, "data": { "key": "I3J525JN", "version": 18, "itemType": "journalArticle", "title": "Furfuryl alcohol polymerisation inside capillaries", "creators": [ { "creatorType": "author", "firstName": "Paulo dos Santos", "lastName": "Batista" }, { "creatorType": "author", "firstName": "Milton Ferreira", "lastName": "de Souza" } ], "abstractNote": "Furfuryl alcohol, FA, oligomer polymerisation was achieved through catalysation by hydrochloric acid, HA, under two different conditions: 1) by HA vapours on the open surface of capillaries containing pure fresh distilled FA and 2) by bubbling a mixture of dry N2 gas and HA solution vapor through a bulk volume of FA. Polymerisation in the capillariesproduces coloured oligomer pellicles that falls under the action of gravity, while the ones generated by the second process do-not fall even under centrifugation. The optical absorption spectra of these oligomers are sensitive to the processing conditions-and capillary diameter. Capillary polymerisation is richer in oligomers of lower molecular weight; the 932nm absorption band being absent. A new optical absorption band at 345nm was measured associated with the water reaction product. Our results indicate that capillary polymerisation is a method that can control conjugated oligomer molecular weight distribution.", "publicationTitle": "Synthetic Metals", "publisher": "", "place": "", "date": "May 1999", "volume": "101", "issue": "1–3", "section": "", "partNumber": "", "partTitle": "", "pages": "635-636", "series": "International Conference on Science and Technology of Synthetic", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "Synthetic Metals", "DOI": "10.1016/S0379-6779(98)00822-4", "citationKey": "", "url": "http://www.sciencedirect.com/science/article/pii/S0379677998008224", "accessDate": "2015-08-25T23:04:21Z", "PMID": "", "PMCID": "", "ISSN": "0379-6779", "archive": "", "archiveLocation": "", "shortTitle": "", "language": "", "libraryCatalog": "ScienceDirect", "callNumber": "", "rights": "", "extra": "", "tags": [ { "tag": "Heterocycle synthesis", "type": 1 }, { "tag": "UV-Vis-NIR absorption", "type": 1 }, { "tag": "liquid surface", "type": 1 }, { "tag": "micellees and solution self-assembly", "type": 1 }, { "tag": "other conjugated and/ or conducting polymers", "type": 1 }, { "tag": "solution processing", "type": 1 } ], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:04:21Z", "dateModified": "2015-08-25T23:04:21Z" } }, { "key": "2Z6VDAJ9", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/2Z6VDAJ9", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/2Z6VDAJ9", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/I3J525JN", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { 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"alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/9HGS8KDD", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/KCVX26N8", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "9HGS8KDD", "version": 18, "parentItem": "KCVX26N8", "itemType": "attachment", "linkMode": "linked_url", "title": "ScienceDirect Full Text PDF", "accessDate": "2015-08-25T23:04:13Z", "url": "http://www.sciencedirect.com/science/article/pii/S0014305701000908/pdfft?md5=3b2ec9a4554d3808c3a488c5d18bb1ca&pid=1-s2.0-S0014305701000908-main.pdf", "note": "", "contentType": "application/pdf", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:04:13Z", "dateModified": "2015-08-25T23:04:13Z" } }, { "key": "PEUQPN7X", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/PEUQPN7X", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/PEUQPN7X", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/KCVX26N8", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "PEUQPN7X", "version": 18, "parentItem": "KCVX26N8", "itemType": "attachment", "linkMode": "linked_url", "title": "ScienceDirect Snapshot", "accessDate": "2015-08-25T23:04:13Z", "url": "http://www.sciencedirect.com/science/article/pii/S0014305701000908", "note": "", "contentType": "text/html", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:04:13Z", "dateModified": "2015-08-25T23:04:13Z" } }, { "key": "KCVX26N8", "version": 18, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/KCVX26N8", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/KCVX26N8", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "González et al.", "parsedDate": "2002-02", "numChildren": 2 }, "data": { "key": "KCVX26N8", "version": 18, "itemType": "journalArticle", "title": "Furfuryl alcohol polymerisation by iodine in methylene chloride", "creators": [ { "creatorType": "author", "firstName": "Regino", "lastName": "González" }, { "creatorType": "author", "firstName": "Juan M.", "lastName": "Figueroa" }, { "creatorType": "author", "firstName": "Hilda", "lastName": "González" } ], "abstractNote": "Furfuryl alcohol (FA) was polymerised by iodine in methylene chloride to give a coloured, amorphous and branched polymer. Structure of FA polymers obtained with iodine have no significant differences according to the IR and NMR spectra respect to those obtained by using Brönsted or Lewis acids as initiators. Changes on the experimental conditions, such as the presence of air, iodine concentration or reaction temperature, did not lead to an increase in the linear structure of the polymer. On the contrary, an increase in the iodine concentration or in the temperature produces a highly crosslinked polymer. DSC of the polymer indicates that remaining groups are able to undergo further exothermic reactions and crosslinking. A mechanism of polymerisation was proposed to explain all the above features.", "publicationTitle": "European Polymer Journal", "publisher": "", "place": "", "date": "February 2002", "volume": "38", "issue": "2", "section": "", "partNumber": "", "partTitle": "", "pages": "287-297", "series": "", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "European Polymer Journal", "DOI": "10.1016/S0014-3057(01)00090-8", "citationKey": "", "url": "http://www.sciencedirect.com/science/article/pii/S0014305701000908", "accessDate": "2015-08-25T23:04:13Z", "PMID": "", "PMCID": "", "ISSN": "0014-3057", "archive": "", "archiveLocation": "", "shortTitle": "", "language": "", "libraryCatalog": "ScienceDirect", "callNumber": "", "rights": "", "extra": "", "tags": [ { "tag": "Amorphous structure", "type": 1 }, { "tag": "Branched structures", "type": 1 }, { "tag": "Polyfurfuryl alcohol", "type": 1 }, { "tag": "Polyunsaturated sequences", "type": 1 }, { "tag": "Pseudocationic polymerisation", "type": 1 }, { "tag": "Reaction mechanism", "type": 1 } ], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:04:13Z", "dateModified": "2015-08-25T23:04:13Z" } }, { "key": "HT57B7SB", "version": 17, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/HT57B7SB", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/HT57B7SB", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/ZJBURU9Q", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "HT57B7SB", "version": 17, "parentItem": "ZJBURU9Q", "itemType": "attachment", "linkMode": "linked_url", "title": "Full Text PDF", "accessDate": "2015-08-25T23:02:33Z", "url": "http://www.tandfonline.com/doi/pdf/10.1080/02773818508085184", "note": "", "contentType": "application/pdf", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:02:33Z", "dateModified": "2015-08-25T23:02:33Z" } }, { "key": "ZJBURU9Q", "version": 17, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/ZJBURU9Q", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/ZJBURU9Q", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Foo and Hemingway", "parsedDate": "1985-01-01", "numChildren": 2 }, "data": { "key": "ZJBURU9Q", "version": 17, "itemType": "journalArticle", "title": "Condensed Tannins: Reactions of Model Compounds with Furfuryl Alcohol and Furfuraldehyde", "creators": [ { "creatorType": "author", "firstName": "L. Yeap", "lastName": "Foo" }, { "creatorType": "author", "firstName": "Richard W.", "lastName": "Hemingway" } ], "abstractNote": "Reaction products of phloroglucinol or catechin with furfuryl alcohol and furfuraldehyde were studied. In reactions of furfuryl alcohol with phloroglucinol, only 2-furyl-1′,3′,5′-trihydroxyphenyl) methane was obtained as product, and 53% of the phloroglucinol was recovered. Reactions of furfuryl alcohol with catechin gave 2-furyl-(8-catechinyl) methane and 2-furyl-(6-catechinyl) methane in 4.0% and 1.5% yields, respectively, while 62% of the catechin was unreacted. Polymeric furans with few catechin moieties made up the oligomeric products (38% of catechin). Reaction of phloroglucinol with furfuraldehyde gave 2-furyl-di(1′,3′,5′-trihydroxyphenyl) methane, an unstable product that readily polymerized during isolation. The solid state 13C-NMR spectrum of the higher polymers suggested one phloroglucinol moiety per furan unit, but lower oligomers contained more furan-furan condensation products. Reactions of catechin with furfuraldehyde gave 2-furyl-di(8-cate-chinyl) methane and the two diastereomers of 2-furyl-(6-catechinyl)-(8-catechinyl) methane in low yield, with 65% of the catechin unreacted.", "publicationTitle": "Journal of Wood Chemistry and Technology", "publisher": "", "place": "", "date": "January 1, 1985", "volume": "5", "issue": "1", "section": "", "partNumber": "", "partTitle": "", "pages": "135-158", "series": "", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "", "DOI": "10.1080/02773818508085184", "citationKey": "", "url": "http://dx.doi.org/10.1080/02773818508085184", "accessDate": "2015-08-25T23:02:33Z", "PMID": "", "PMCID": "", "ISSN": "0277-3813", "archive": "", "archiveLocation": "", "shortTitle": "Condensed Tannins", "language": "", "libraryCatalog": "Taylor and Francis+NEJM", "callNumber": "", "rights": "", "extra": "", "tags": [], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:02:33Z", "dateModified": "2015-08-25T23:02:33Z" } }, { "key": "R3B3RHPS", "version": 17, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/R3B3RHPS", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/R3B3RHPS", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/ZJBURU9Q", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "R3B3RHPS", "version": 17, "parentItem": "ZJBURU9Q", "itemType": "attachment", "linkMode": "linked_url", "title": "Snapshot", "accessDate": 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"https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "GSNEA859", "version": 16, "parentItem": "KW6F799I", "itemType": "attachment", "linkMode": "linked_url", "title": "Snapshot", "accessDate": "2015-08-25T23:01:46Z", "url": "http://onlinelibrary.wiley.com/doi/10.1897/04-243R.1/full", "note": "", "contentType": "text/html", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:01:46Z", "dateModified": "2015-08-25T23:01:46Z" } }, { "key": "KW6F799I", "version": 16, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/KW6F799I", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/KW6F799I", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Latch et al.", "parsedDate": "2005-03-01", "numChildren": 2 }, "data": { "key": "KW6F799I", "version": 16, "itemType": "journalArticle", "title": "Aqueous photochemistry of triclosan: Formation of 2,4-dichlorophenol, 2,8-dichlorodibenzo-p-dioxin, and oligomerization products", "creators": [ { "creatorType": "author", "firstName": "Douglas E.", "lastName": "Latch" }, { "creatorType": "author", "firstName": "Jennifer L.", "lastName": "Packer" }, { "creatorType": "author", "firstName": "Brian L.", "lastName": "Stender" }, { "creatorType": "author", "firstName": "Jennifer", "lastName": "VanOverbeke" }, { "creatorType": "author", "firstName": "William A.", "lastName": "Arnold" }, { "creatorType": "author", "firstName": "Kristopher", "lastName": "McNeill" } ], "abstractNote": "The photochemical fate of the antimicrobial agent triclosan is presented. Experiments performed in both natural and buffered deionized water show that triclosan rapidly photodegrades by direct photolysis (t½ = 5 h, pH 8, noon summer sunlight, 45°N latitude). Both 2,8-dichlorodibenzo-p-dioxin (2,8-DCDD) and 2,4-dichlorophenol (2,4-DCP) are produced. The 2,8-DCDD and 2,4-DCP also are photolabile and, thus, are intermediates. The yields for 2,8-DCDD and 2,4-DCP ranged from 3 to 12% depending on the conditions employed. When triclosan is photolyzed in the presence of Suwannee River (GA, USA) fulvic acid, a portion of the initial mass is recovered as insoluble material. Based on experiments in which the formation of insoluble material was monitored with photolysis time, it is postulated that photolysis in natural waters leads to some of the triclosan being coupled to humic matter. Triclosan also reacts rapidly with both singlet oxygen (krxn = 1.07 ± 0.03 × 108 M−1 s−1 in water of pH 10) and hydroxyl radical (k·OH = 5.4 ± 0.3 × 109 M−1 s−1). Indirect photolysis pathways, however, are not expected to be important because of low steady-state concentrations of reactive oxygen species in natural waters and the efficiency of the direct photolysis of triclosan.", "publicationTitle": "Environmental Toxicology and Chemistry", "publisher": "", "place": "", "date": "March 1, 2005", "volume": "24", "issue": "3", "section": "", "partNumber": "", "partTitle": "", "pages": "517-525", "series": "", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "Environmental Toxicology and Chemistry", "DOI": "10.1897/04-243R.1", "citationKey": "", "url": "http://onlinelibrary.wiley.com/doi/10.1897/04-243R.1/abstract", "accessDate": "2015-08-25T23:01:46Z", "PMID": "", "PMCID": "", "ISSN": "1552-8618", "archive": "", "archiveLocation": "", "shortTitle": "Aqueous photochemistry of triclosan", "language": "en", "libraryCatalog": "Wiley Online Library", "callNumber": "", "rights": "Copyright © 2005 SETAC", "extra": "", "tags": [ { "tag": "Dichlorophenol", "type": 1 }, { "tag": "Dioxin", "type": 1 }, { "tag": "Photochemistry", "type": 1 }, { "tag": "Reactive oxygen species", "type": 1 }, { "tag": "Triclosan", "type": 1 } ], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:01:46Z", "dateModified": "2015-08-25T23:01:46Z" } }, { "key": "6ABSGQ45", "version": 16, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/6ABSGQ45", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/6ABSGQ45", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/KW6F799I", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", 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"http://www.sciencedirect.com/science/article/pii/S000862230500117X", "note": "", "contentType": "text/html", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:01:20Z", "dateModified": "2015-08-25T23:01:20Z" } }, { "key": "3B3USUHC", "version": 15, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/3B3USUHC", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/3B3USUHC", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Yao et al.", "parsedDate": "2005-07", "numChildren": 2 }, "data": { "key": "3B3USUHC", "version": 15, "itemType": "journalArticle", "title": "Preparation of colloidal microporous carbon spheres from furfuryl alcohol", "creators": [ { "creatorType": "author", "firstName": "Jianfeng", "lastName": "Yao" }, { "creatorType": "author", "firstName": "Huanting", "lastName": "Wang" }, { "creatorType": "author", "firstName": "Jin", "lastName": "Liu" }, { "creatorType": "author", "firstName": "Kwong-Yu", "lastName": "Chan" }, { "creatorType": "author", "firstName": "Lixiong", "lastName": "Zhang" }, { "creatorType": "author", "firstName": "Nanping", "lastName": "Xu" } ], "abstractNote": "Colloidal microporous carbon (MC) spheres with an average size of 260 nm–1.5 μm were prepared by carbonization of “nonstick” poly(furfuryl alcohol) (PFA) spheres, which were synthesized by a two-step polymerization of furfuryl alcohol (FA) involving slow polymerization (1st step) and sphere formation (2nd step). The high dispersibility of the MC spheres was simultaneously realized by removing surface functional groups of the PFA spheres with the evaporation-induced concentrated sulfuric acid (2nd step). By varying the temperature of slow polymerization, the spheres with different sizes could be simply synthesized. The studies also showed that surfactant and sulfuric acid treatment played an important role in the synthesis of colloidal PFA (MC) spheres.", "publicationTitle": "Carbon", "publisher": "", "place": "", "date": "July 2005", "volume": "43", "issue": "8", "section": "", "partNumber": "", "partTitle": "", "pages": "1709-1715", "series": "", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "Carbon", "DOI": "10.1016/j.carbon.2005.02.014", "citationKey": "", "url": "http://www.sciencedirect.com/science/article/pii/S000862230500117X", "accessDate": "2015-08-25T23:01:20Z", "PMID": "", "PMCID": "", "ISSN": "0008-6223", "archive": "", "archiveLocation": "", "shortTitle": "", "language": "", "libraryCatalog": "ScienceDirect", "callNumber": "", "rights": "", "extra": "", "tags": [ { "tag": "Carbonization", "type": 1 }, { "tag": "Particle size", "type": 1 }, { "tag": "Porous carbon", "type": 1 } ], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:01:20Z", "dateModified": "2015-08-25T23:01:20Z" } }, { "key": "5E6DES8J", "version": 14, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/5E6DES8J", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/5E6DES8J", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/D7GVWZ56", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "5E6DES8J", "version": 14, "parentItem": "D7GVWZ56", "itemType": "attachment", "linkMode": "linked_url", "title": "ScienceDirect Full Text PDF", "accessDate": "2015-08-25T23:00:57Z", "url": "http://www.sciencedirect.com/science/article/pii/S0032386100001786/pdfft?md5=8a513aeec3d104ecbe776b6ecbb8fba0&pid=1-s2.0-S0032386100001786-main.pdf", "note": "", "contentType": "application/pdf", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:00:57Z", "dateModified": "2015-08-25T23:00:57Z" } }, { "key": "QDI5SA7X", "version": 14, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/QDI5SA7X", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/QDI5SA7X", "type": "text/html" }, "up": { "href": "https://api.zotero.org/groups/389114/items/D7GVWZ56", "type": "application/json" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } } }, "data": { "key": "QDI5SA7X", "version": 14, "parentItem": "D7GVWZ56", "itemType": "attachment", "linkMode": "linked_url", "title": "ScienceDirect Snapshot", "accessDate": "2015-08-25T23:00:57Z", "url": "http://www.sciencedirect.com/science/article/pii/S0032386100001786", "note": "", "contentType": "text/html", "charset": "", "tags": [], "relations": {}, "dateAdded": "2015-08-25T23:00:57Z", "dateModified": "2015-08-25T23:00:57Z" } }, { "key": "D7GVWZ56", "version": 14, "library": { "type": "group", "id": 389114, "name": "Furfuryl Alcohol and Oligomerization", "links": { "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization", "type": "text/html" } } }, "links": { "self": { "href": "https://api.zotero.org/groups/389114/items/D7GVWZ56", "type": "application/json" }, "alternate": { "href": "https://www.zotero.org/groups/furfuryl_alcohol_and_oligomerization/items/D7GVWZ56", "type": "text/html" } }, "meta": { "createdByUser": { "id": 1989183, "username": "rachel.desormes", "name": "", "links": { "alternate": { "href": "https://www.zotero.org/rachel.desormes", "type": "text/html" } } }, "creatorSummary": "Batista and de Souza", "parsedDate": "2000-11", "numChildren": 2 }, "data": { "key": "D7GVWZ56", "version": 14, "itemType": "journalArticle", "title": "Furfuryl alcohol conjugated oligomer pellicle formation", "creators": [ { "creatorType": "author", "firstName": "P. S.", "lastName": "Batista" }, { "creatorType": "author", "firstName": "M. F.", "lastName": "de Souza" } ], "abstractNote": "The heterogeneous acid catalysis of furfurylic alcohol oligomer polymerisation was investigated for the first time. Oligomer conjugated bond structures were confirmed through their optical absorption bands at 570, 650, 770 and 930 nm. Polymerisation in the furfurylic alcohol surface inside glass tubes produced porous pellicles that fell as a result of gravity, breaking apart when tube radii were larger than 0.27 cm. The high oligomer concentration at the furfurylic alcohol surface caused the formation of oligomer clusters that bound to each other to generate the porous and electrically conductive pellicle. Oligomers produced by heterogeneous catalysis have a molecular weight distribution richer in small oligomers than those produced by homogeneous catalysis.", "publicationTitle": "Polymer", "publisher": "", "place": "", "date": "November 2000", "volume": "41", "issue": "23", "section": "", "partNumber": "", "partTitle": "", "pages": "8263-8269", "series": "", "seriesTitle": "", "seriesText": "", "journalAbbreviation": "Polymer", "DOI": "10.1016/S0032-3861(00)00178-6", "citationKey": "", "url": "http://www.sciencedirect.com/science/article/pii/S0032386100001786", "accessDate": "2015-08-25T23:00:57Z", "PMID": "", "PMCID": "", "ISSN": "0032-3861", "archive": "", "archiveLocation": "", "shortTitle": "", "language": "", "libraryCatalog": "ScienceDirect", "callNumber": "", "rights": "", "extra": "", "tags": [ { "tag": "Conjugate oligomers", "type": 1 }, { "tag": "Furfurylic alcohol", "type": 1 }, { "tag": "heterogeneous catalysis", "type": 1 } ], "collections": [], "relations": {}, "dateAdded": "2015-08-25T23:00:57Z", "dateModified": "2015-08-25T23:00:57Z" } } ]