Loading…
Synthesis of porphyrin-dendrimers with a pyrene in the periphery and their cubic nonlinear optical properties
Dendrons of pyrene derivatives were attached to a porphyrin core. A marked effect in solution for the dendrimers was observed in the absorption spectra. All the compounds obtained were characterized by (1)H-, (13)C-NMR, FTIR, UV-vis, MALDI-TOF or FAB+ mass spectrometry and elemental analysis. The cu...
Saved in:
Published in: | Molecules (Basel, Switzerland) Switzerland), 2011-08, Vol.16 (8), p.6950-6968 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c492t-fcc71e67819e697ae747337266eafdcc8e14b276a0deb44622eca53cb916cfd33 |
---|---|
cites | cdi_FETCH-LOGICAL-c492t-fcc71e67819e697ae747337266eafdcc8e14b276a0deb44622eca53cb916cfd33 |
container_end_page | 6968 |
container_issue | 8 |
container_start_page | 6950 |
container_title | Molecules (Basel, Switzerland) |
container_volume | 16 |
creator | Morales-Espinoza, Eric G Lijanova, Irina V Morales-Saavedra, Omar G Torres-Zuñiga, Vícente Hernandez-Ortega, Simon Martínez-García, Marcos |
description | Dendrons of pyrene derivatives were attached to a porphyrin core. A marked effect in solution for the dendrimers was observed in the absorption spectra. All the compounds obtained were characterized by (1)H-, (13)C-NMR, FTIR, UV-vis, MALDI-TOF or FAB+ mass spectrometry and elemental analysis. The cubic nonlinear optical behavior of some the synthesized compounds was tested via Z-Scan measurements in spin-coated film samples. |
doi_str_mv | 10.3390/molecules16086950 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_edfc5b6c957d4ba19d0edfb8adbd95a6</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_edfc5b6c957d4ba19d0edfb8adbd95a6</doaj_id><sourcerecordid>3323146951</sourcerecordid><originalsourceid>FETCH-LOGICAL-c492t-fcc71e67819e697ae747337266eafdcc8e14b276a0deb44622eca53cb916cfd33</originalsourceid><addsrcrecordid>eNplkU1rFjEUhQdRbK3-ADcScD01X5OZbIRS1BYKXVTXIR93OnmZN4nJTMv8e1PfWlpcJZyc--QeTtN8JPiUMYm_7OMMdp2hEIEHITv8qjkmnOKWYS5fP7sfNe9K2WFMCSfd2-aIkoHzgbPjZn-zhWWC4guKI0oxp2nLPrQOgst-D7mge79MSKO0ZQiAfEDVjxJknybIG9LBPSg-I7sab1GIYfYBdEYxLd7qGaUcq33xUN43b0Y9F_jweJ40v75_-3l-0V5d_7g8P7tqLZd0aUdrewKiH4gEIXsNPe8Z66kQoEdn7QCEG9oLjR0YzgWlYHXHrJFE2NExdtJcHrgu6p1KNYjOm4raq79CzLdK14XsDArcaDsjrOx6x40m0uEqmUE742SnRWV9PbDSavbgLIQl6_kF9OVL8JO6jXdKUMGJHCrg8yMgx98rlEXt4ppDza9Ix4iokTmuLnJw2RxLyTA-_UCwemhb_dd2nfn0fLWniX_1sj_Ui6z0</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1531649240</pqid></control><display><type>article</type><title>Synthesis of porphyrin-dendrimers with a pyrene in the periphery and their cubic nonlinear optical properties</title><source>PubMed (Medline)</source><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><creator>Morales-Espinoza, Eric G ; Lijanova, Irina V ; Morales-Saavedra, Omar G ; Torres-Zuñiga, Vícente ; Hernandez-Ortega, Simon ; Martínez-García, Marcos</creator><creatorcontrib>Morales-Espinoza, Eric G ; Lijanova, Irina V ; Morales-Saavedra, Omar G ; Torres-Zuñiga, Vícente ; Hernandez-Ortega, Simon ; Martínez-García, Marcos</creatorcontrib><description>Dendrons of pyrene derivatives were attached to a porphyrin core. A marked effect in solution for the dendrimers was observed in the absorption spectra. All the compounds obtained were characterized by (1)H-, (13)C-NMR, FTIR, UV-vis, MALDI-TOF or FAB+ mass spectrometry and elemental analysis. The cubic nonlinear optical behavior of some the synthesized compounds was tested via Z-Scan measurements in spin-coated film samples.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules16086950</identifier><identifier>PMID: 21844843</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Alcohol ; Chemistry, Organic - methods ; Crystal structure ; dendrimers ; Dendrimers - chemical synthesis ; Magnetic Resonance Spectroscopy ; Mass spectrometry ; Molecular Probes - chemical synthesis ; nonlinear optics ; Optical Phenomena ; Optical properties ; Organic light emitting diodes ; porphyrin ; Porphyrins - chemical synthesis ; pyrene ; Pyrenes - chemistry ; Scientific imaging ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Spectrophotometry, Ultraviolet ; Spectroscopy, Fourier Transform Infrared</subject><ispartof>Molecules (Basel, Switzerland), 2011-08, Vol.16 (8), p.6950-6968</ispartof><rights>Copyright MDPI AG 2011</rights><rights>2011 by the authors; 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c492t-fcc71e67819e697ae747337266eafdcc8e14b276a0deb44622eca53cb916cfd33</citedby><cites>FETCH-LOGICAL-c492t-fcc71e67819e697ae747337266eafdcc8e14b276a0deb44622eca53cb916cfd33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1531649240/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1531649240?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21844843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morales-Espinoza, Eric G</creatorcontrib><creatorcontrib>Lijanova, Irina V</creatorcontrib><creatorcontrib>Morales-Saavedra, Omar G</creatorcontrib><creatorcontrib>Torres-Zuñiga, Vícente</creatorcontrib><creatorcontrib>Hernandez-Ortega, Simon</creatorcontrib><creatorcontrib>Martínez-García, Marcos</creatorcontrib><title>Synthesis of porphyrin-dendrimers with a pyrene in the periphery and their cubic nonlinear optical properties</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>Dendrons of pyrene derivatives were attached to a porphyrin core. A marked effect in solution for the dendrimers was observed in the absorption spectra. All the compounds obtained were characterized by (1)H-, (13)C-NMR, FTIR, UV-vis, MALDI-TOF or FAB+ mass spectrometry and elemental analysis. The cubic nonlinear optical behavior of some the synthesized compounds was tested via Z-Scan measurements in spin-coated film samples.</description><subject>Alcohol</subject><subject>Chemistry, Organic - methods</subject><subject>Crystal structure</subject><subject>dendrimers</subject><subject>Dendrimers - chemical synthesis</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mass spectrometry</subject><subject>Molecular Probes - chemical synthesis</subject><subject>nonlinear optics</subject><subject>Optical Phenomena</subject><subject>Optical properties</subject><subject>Organic light emitting diodes</subject><subject>porphyrin</subject><subject>Porphyrins - chemical synthesis</subject><subject>pyrene</subject><subject>Pyrenes - chemistry</subject><subject>Scientific imaging</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkU1rFjEUhQdRbK3-ADcScD01X5OZbIRS1BYKXVTXIR93OnmZN4nJTMv8e1PfWlpcJZyc--QeTtN8JPiUMYm_7OMMdp2hEIEHITv8qjkmnOKWYS5fP7sfNe9K2WFMCSfd2-aIkoHzgbPjZn-zhWWC4guKI0oxp2nLPrQOgst-D7mge79MSKO0ZQiAfEDVjxJknybIG9LBPSg-I7sab1GIYfYBdEYxLd7qGaUcq33xUN43b0Y9F_jweJ40v75_-3l-0V5d_7g8P7tqLZd0aUdrewKiH4gEIXsNPe8Z66kQoEdn7QCEG9oLjR0YzgWlYHXHrJFE2NExdtJcHrgu6p1KNYjOm4raq79CzLdK14XsDArcaDsjrOx6x40m0uEqmUE742SnRWV9PbDSavbgLIQl6_kF9OVL8JO6jXdKUMGJHCrg8yMgx98rlEXt4ppDza9Ix4iokTmuLnJw2RxLyTA-_UCwemhb_dd2nfn0fLWniX_1sj_Ui6z0</recordid><startdate>20110815</startdate><enddate>20110815</enddate><creator>Morales-Espinoza, Eric G</creator><creator>Lijanova, Irina V</creator><creator>Morales-Saavedra, Omar G</creator><creator>Torres-Zuñiga, Vícente</creator><creator>Hernandez-Ortega, Simon</creator><creator>Martínez-García, Marcos</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110815</creationdate><title>Synthesis of porphyrin-dendrimers with a pyrene in the periphery and their cubic nonlinear optical properties</title><author>Morales-Espinoza, Eric G ; Lijanova, Irina V ; Morales-Saavedra, Omar G ; Torres-Zuñiga, Vícente ; Hernandez-Ortega, Simon ; Martínez-García, Marcos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c492t-fcc71e67819e697ae747337266eafdcc8e14b276a0deb44622eca53cb916cfd33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Alcohol</topic><topic>Chemistry, Organic - methods</topic><topic>Crystal structure</topic><topic>dendrimers</topic><topic>Dendrimers - chemical synthesis</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Mass spectrometry</topic><topic>Molecular Probes - chemical synthesis</topic><topic>nonlinear optics</topic><topic>Optical Phenomena</topic><topic>Optical properties</topic><topic>Organic light emitting diodes</topic><topic>porphyrin</topic><topic>Porphyrins - chemical synthesis</topic><topic>pyrene</topic><topic>Pyrenes - chemistry</topic><topic>Scientific imaging</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morales-Espinoza, Eric G</creatorcontrib><creatorcontrib>Lijanova, Irina V</creatorcontrib><creatorcontrib>Morales-Saavedra, Omar G</creatorcontrib><creatorcontrib>Torres-Zuñiga, Vícente</creatorcontrib><creatorcontrib>Hernandez-Ortega, Simon</creatorcontrib><creatorcontrib>Martínez-García, Marcos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morales-Espinoza, Eric G</au><au>Lijanova, Irina V</au><au>Morales-Saavedra, Omar G</au><au>Torres-Zuñiga, Vícente</au><au>Hernandez-Ortega, Simon</au><au>Martínez-García, Marcos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of porphyrin-dendrimers with a pyrene in the periphery and their cubic nonlinear optical properties</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2011-08-15</date><risdate>2011</risdate><volume>16</volume><issue>8</issue><spage>6950</spage><epage>6968</epage><pages>6950-6968</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>Dendrons of pyrene derivatives were attached to a porphyrin core. A marked effect in solution for the dendrimers was observed in the absorption spectra. All the compounds obtained were characterized by (1)H-, (13)C-NMR, FTIR, UV-vis, MALDI-TOF or FAB+ mass spectrometry and elemental analysis. The cubic nonlinear optical behavior of some the synthesized compounds was tested via Z-Scan measurements in spin-coated film samples.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>21844843</pmid><doi>10.3390/molecules16086950</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1420-3049 |
ispartof | Molecules (Basel, Switzerland), 2011-08, Vol.16 (8), p.6950-6968 |
issn | 1420-3049 1420-3049 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_edfc5b6c957d4ba19d0edfb8adbd95a6 |
source | PubMed (Medline); Publicly Available Content Database (Proquest) (PQ_SDU_P3) |
subjects | Alcohol Chemistry, Organic - methods Crystal structure dendrimers Dendrimers - chemical synthesis Magnetic Resonance Spectroscopy Mass spectrometry Molecular Probes - chemical synthesis nonlinear optics Optical Phenomena Optical properties Organic light emitting diodes porphyrin Porphyrins - chemical synthesis pyrene Pyrenes - chemistry Scientific imaging Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Spectrophotometry, Ultraviolet Spectroscopy, Fourier Transform Infrared |
title | Synthesis of porphyrin-dendrimers with a pyrene in the periphery and their cubic nonlinear optical properties |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T14%3A18%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20porphyrin-dendrimers%20with%20a%20pyrene%20in%20the%20periphery%20and%20their%20cubic%20nonlinear%20optical%20properties&rft.jtitle=Molecules%20(Basel,%20Switzerland)&rft.au=Morales-Espinoza,%20Eric%20G&rft.date=2011-08-15&rft.volume=16&rft.issue=8&rft.spage=6950&rft.epage=6968&rft.pages=6950-6968&rft.issn=1420-3049&rft.eissn=1420-3049&rft_id=info:doi/10.3390/molecules16086950&rft_dat=%3Cproquest_doaj_%3E3323146951%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c492t-fcc71e67819e697ae747337266eafdcc8e14b276a0deb44622eca53cb916cfd33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1531649240&rft_id=info:pmid/21844843&rfr_iscdi=true |