Thermal studies of hypervalent iodine reagents
Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-suppo...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Verma, Vikas [verfasserIn] |
|---|
| Format: |
Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2013 |
|---|
| Schlagwörter: |
|---|
| Anmerkung: |
© Akadémiai Kiadó, Budapest, Hungary 2013 |
|---|
| Übergeordnetes Werk: |
Enthalten in: Journal of thermal analysis and calorimetry - Springer Netherlands, 1998, 114(2013), 1 vom: 13. Jan., Seite 339-344 |
|---|---|
| Übergeordnetes Werk: |
volume:114 ; year:2013 ; number:1 ; day:13 ; month:01 ; pages:339-344 |
| Links: |
|---|
| DOI / URN: |
10.1007/s10973-012-2894-1 |
|---|
| Katalog-ID: |
OLC2049823762 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | OLC2049823762 | ||
| 003 | DE-627 | ||
| 005 | 20230503165859.0 | ||
| 007 | tu | ||
| 008 | 200820s2013 xx ||||| 00| ||eng c | ||
| 024 | 7 | |a 10.1007/s10973-012-2894-1 |2 doi | |
| 035 | |a (DE-627)OLC2049823762 | ||
| 035 | |a (DE-He213)s10973-012-2894-1-p | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 082 | 0 | 4 | |a 660 |q VZ |
| 100 | 1 | |a Verma, Vikas |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Thermal studies of hypervalent iodine reagents |
| 264 | 1 | |c 2013 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
| 338 | |a Band |b nc |2 rdacarrier | ||
| 500 | |a © Akadémiai Kiadó, Budapest, Hungary 2013 | ||
| 520 | |a Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. | ||
| 650 | 4 | |a Hypervalent iodine reagents | |
| 650 | 4 | |a Polymer-supported hypervalent iodine reagents | |
| 650 | 4 | |a DSC | |
| 650 | 4 | |a TG | |
| 700 | 1 | |a Singh, Kuldeep |4 aut | |
| 700 | 1 | |a Kumar, Ashok |4 aut | |
| 700 | 1 | |a Kumar, Devinder |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Journal of thermal analysis and calorimetry |d Springer Netherlands, 1998 |g 114(2013), 1 vom: 13. Jan., Seite 339-344 |w (DE-627)244148767 |w (DE-600)1429493-X |w (DE-576)066397693 |x 1388-6150 |7 nnns |
| 773 | 1 | 8 | |g volume:114 |g year:2013 |g number:1 |g day:13 |g month:01 |g pages:339-344 |
| 856 | 4 | 1 | |u https://doi.org/10.1007/s10973-012-2894-1 |z lizenzpflichtig |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a SYSFLAG_A | ||
| 912 | |a GBV_OLC | ||
| 912 | |a SSG-OLC-TEC | ||
| 912 | |a SSG-OLC-CHE | ||
| 912 | |a GBV_ILN_70 | ||
| 951 | |a AR | ||
| 952 | |d 114 |j 2013 |e 1 |b 13 |c 01 |h 339-344 | ||
| author_variant |
v v vv k s ks a k ak d k dk |
|---|---|
| matchkey_str |
article:13886150:2013----::hrasuisfyevlnid |
| hierarchy_sort_str |
2013 |
| publishDate |
2013 |
| allfields |
10.1007/s10973-012-2894-1 doi (DE-627)OLC2049823762 (DE-He213)s10973-012-2894-1-p DE-627 ger DE-627 rakwb eng 660 VZ Verma, Vikas verfasserin aut Thermal studies of hypervalent iodine reagents 2013 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2013 Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. Hypervalent iodine reagents Polymer-supported hypervalent iodine reagents DSC TG Singh, Kuldeep aut Kumar, Ashok aut Kumar, Devinder aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 114(2013), 1 vom: 13. Jan., Seite 339-344 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:114 year:2013 number:1 day:13 month:01 pages:339-344 https://doi.org/10.1007/s10973-012-2894-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 114 2013 1 13 01 339-344 |
| spelling |
10.1007/s10973-012-2894-1 doi (DE-627)OLC2049823762 (DE-He213)s10973-012-2894-1-p DE-627 ger DE-627 rakwb eng 660 VZ Verma, Vikas verfasserin aut Thermal studies of hypervalent iodine reagents 2013 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2013 Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. Hypervalent iodine reagents Polymer-supported hypervalent iodine reagents DSC TG Singh, Kuldeep aut Kumar, Ashok aut Kumar, Devinder aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 114(2013), 1 vom: 13. Jan., Seite 339-344 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:114 year:2013 number:1 day:13 month:01 pages:339-344 https://doi.org/10.1007/s10973-012-2894-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 114 2013 1 13 01 339-344 |
| allfields_unstemmed |
10.1007/s10973-012-2894-1 doi (DE-627)OLC2049823762 (DE-He213)s10973-012-2894-1-p DE-627 ger DE-627 rakwb eng 660 VZ Verma, Vikas verfasserin aut Thermal studies of hypervalent iodine reagents 2013 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2013 Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. Hypervalent iodine reagents Polymer-supported hypervalent iodine reagents DSC TG Singh, Kuldeep aut Kumar, Ashok aut Kumar, Devinder aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 114(2013), 1 vom: 13. Jan., Seite 339-344 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:114 year:2013 number:1 day:13 month:01 pages:339-344 https://doi.org/10.1007/s10973-012-2894-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 114 2013 1 13 01 339-344 |
| allfieldsGer |
10.1007/s10973-012-2894-1 doi (DE-627)OLC2049823762 (DE-He213)s10973-012-2894-1-p DE-627 ger DE-627 rakwb eng 660 VZ Verma, Vikas verfasserin aut Thermal studies of hypervalent iodine reagents 2013 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2013 Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. Hypervalent iodine reagents Polymer-supported hypervalent iodine reagents DSC TG Singh, Kuldeep aut Kumar, Ashok aut Kumar, Devinder aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 114(2013), 1 vom: 13. Jan., Seite 339-344 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:114 year:2013 number:1 day:13 month:01 pages:339-344 https://doi.org/10.1007/s10973-012-2894-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 114 2013 1 13 01 339-344 |
| allfieldsSound |
10.1007/s10973-012-2894-1 doi (DE-627)OLC2049823762 (DE-He213)s10973-012-2894-1-p DE-627 ger DE-627 rakwb eng 660 VZ Verma, Vikas verfasserin aut Thermal studies of hypervalent iodine reagents 2013 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2013 Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. Hypervalent iodine reagents Polymer-supported hypervalent iodine reagents DSC TG Singh, Kuldeep aut Kumar, Ashok aut Kumar, Devinder aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 114(2013), 1 vom: 13. Jan., Seite 339-344 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:114 year:2013 number:1 day:13 month:01 pages:339-344 https://doi.org/10.1007/s10973-012-2894-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 114 2013 1 13 01 339-344 |
| language |
English |
| source |
Enthalten in Journal of thermal analysis and calorimetry 114(2013), 1 vom: 13. Jan., Seite 339-344 volume:114 year:2013 number:1 day:13 month:01 pages:339-344 |
| sourceStr |
Enthalten in Journal of thermal analysis and calorimetry 114(2013), 1 vom: 13. Jan., Seite 339-344 volume:114 year:2013 number:1 day:13 month:01 pages:339-344 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| topic_facet |
Hypervalent iodine reagents Polymer-supported hypervalent iodine reagents DSC TG |
| dewey-raw |
660 |
| isfreeaccess_bool |
false |
| container_title |
Journal of thermal analysis and calorimetry |
| authorswithroles_txt_mv |
Verma, Vikas @@aut@@ Singh, Kuldeep @@aut@@ Kumar, Ashok @@aut@@ Kumar, Devinder @@aut@@ |
| publishDateDaySort_date |
2013-01-13T00:00:00Z |
| hierarchy_top_id |
244148767 |
| dewey-sort |
3660 |
| id |
OLC2049823762 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">OLC2049823762</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503165859.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200820s2013 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10973-012-2894-1</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2049823762</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)s10973-012-2894-1-p</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">660</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Verma, Vikas</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Thermal studies of hypervalent iodine reagents</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2013</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Akadémiai Kiadó, Budapest, Hungary 2013</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Hypervalent iodine reagents</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Polymer-supported hypervalent iodine reagents</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">DSC</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">TG</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Singh, Kuldeep</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kumar, Ashok</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kumar, Devinder</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of thermal analysis and calorimetry</subfield><subfield code="d">Springer Netherlands, 1998</subfield><subfield code="g">114(2013), 1 vom: 13. Jan., Seite 339-344</subfield><subfield code="w">(DE-627)244148767</subfield><subfield code="w">(DE-600)1429493-X</subfield><subfield code="w">(DE-576)066397693</subfield><subfield code="x">1388-6150</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:114</subfield><subfield code="g">year:2013</subfield><subfield code="g">number:1</subfield><subfield code="g">day:13</subfield><subfield code="g">month:01</subfield><subfield code="g">pages:339-344</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/s10973-012-2894-1</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">114</subfield><subfield code="j">2013</subfield><subfield code="e">1</subfield><subfield code="b">13</subfield><subfield code="c">01</subfield><subfield code="h">339-344</subfield></datafield></record></collection>
|
| author |
Verma, Vikas |
| spellingShingle |
Verma, Vikas ddc 660 misc Hypervalent iodine reagents misc Polymer-supported hypervalent iodine reagents misc DSC misc TG Thermal studies of hypervalent iodine reagents |
| authorStr |
Verma, Vikas |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)244148767 |
| format |
Article |
| dewey-ones |
660 - Chemical engineering |
| delete_txt_mv |
keep |
| author_role |
aut aut aut aut |
| collection |
OLC |
| remote_str |
false |
| illustrated |
Not Illustrated |
| issn |
1388-6150 |
| topic_title |
660 VZ Thermal studies of hypervalent iodine reagents Hypervalent iodine reagents Polymer-supported hypervalent iodine reagents DSC TG |
| topic |
ddc 660 misc Hypervalent iodine reagents misc Polymer-supported hypervalent iodine reagents misc DSC misc TG |
| topic_unstemmed |
ddc 660 misc Hypervalent iodine reagents misc Polymer-supported hypervalent iodine reagents misc DSC misc TG |
| topic_browse |
ddc 660 misc Hypervalent iodine reagents misc Polymer-supported hypervalent iodine reagents misc DSC misc TG |
| format_facet |
Aufsätze Gedruckte Aufsätze |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
nc |
| hierarchy_parent_title |
Journal of thermal analysis and calorimetry |
| hierarchy_parent_id |
244148767 |
| dewey-tens |
660 - Chemical engineering |
| hierarchy_top_title |
Journal of thermal analysis and calorimetry |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 |
| title |
Thermal studies of hypervalent iodine reagents |
| ctrlnum |
(DE-627)OLC2049823762 (DE-He213)s10973-012-2894-1-p |
| title_full |
Thermal studies of hypervalent iodine reagents |
| author_sort |
Verma, Vikas |
| journal |
Journal of thermal analysis and calorimetry |
| journalStr |
Journal of thermal analysis and calorimetry |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
600 - Technology |
| recordtype |
marc |
| publishDateSort |
2013 |
| contenttype_str_mv |
txt |
| container_start_page |
339 |
| author_browse |
Verma, Vikas Singh, Kuldeep Kumar, Ashok Kumar, Devinder |
| container_volume |
114 |
| class |
660 VZ |
| format_se |
Aufsätze |
| author-letter |
Verma, Vikas |
| doi_str_mv |
10.1007/s10973-012-2894-1 |
| dewey-full |
660 |
| title_sort |
thermal studies of hypervalent iodine reagents |
| title_auth |
Thermal studies of hypervalent iodine reagents |
| abstract |
Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. © Akadémiai Kiadó, Budapest, Hungary 2013 |
| abstractGer |
Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. © Akadémiai Kiadó, Budapest, Hungary 2013 |
| abstract_unstemmed |
Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C. © Akadémiai Kiadó, Budapest, Hungary 2013 |
| collection_details |
GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 |
| container_issue |
1 |
| title_short |
Thermal studies of hypervalent iodine reagents |
| url |
https://doi.org/10.1007/s10973-012-2894-1 |
| remote_bool |
false |
| author2 |
Singh, Kuldeep Kumar, Ashok Kumar, Devinder |
| author2Str |
Singh, Kuldeep Kumar, Ashok Kumar, Devinder |
| ppnlink |
244148767 |
| mediatype_str_mv |
n |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| doi_str |
10.1007/s10973-012-2894-1 |
| up_date |
2024-07-04T00:09:20.475Z |
| _version_ |
1803604994793930752 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">OLC2049823762</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503165859.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200820s2013 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10973-012-2894-1</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2049823762</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)s10973-012-2894-1-p</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">660</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Verma, Vikas</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Thermal studies of hypervalent iodine reagents</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2013</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Akadémiai Kiadó, Budapest, Hungary 2013</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract The thermal properties of hypervalent iodine reagents (iodobenzene diacetate, bis(trifluoroacetoxy)iodobenzene, [hydroxyl(mesyloxy)]iodobenzene, [hydroxy(tosyloxy)] iodobenzene) and polymer-supported hypervalent iodine reagents (polystyrene-supported iodobenzene diacetate, polystyrene-supported bis(trifluoroacetoxy)iodobenzene, polystyrene-supported[hydroxyl(mesyloxy)]iodobenzene, polystyrene-supported [hydroxy(tosyloxy)] iodobenzene) were investigated using thermogravimetry (TG) and differential scanning calorimetry (DSC). The polystyrene-supported iodobenzene diacetate, synthesized from polystyrene, was a precursor to other three polymer-supported hypervalent iodine reagents (PS-HTIB, PS-HMIB and PS-BTI). The TG curves of hypervalent iodine reagents and their polymer analogues show mainly one-step mass loss behaviour, whereas enthalpy change (∆H) and onset temperature were calculated from a DSC curve which that shows hypervalent iodine reagents and their polymer analogues decompose endothermically. The results suggest that the polymer-supported hypervalent iodine reagents are more stable than hypervalent iodine reagents and therefore may be used in reactions without decomposition up to 350–410 °C in comparison to the polymer-supported hypervalent iodine reagents that are stable up to 132–160 °C.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Hypervalent iodine reagents</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Polymer-supported hypervalent iodine reagents</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">DSC</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">TG</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Singh, Kuldeep</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kumar, Ashok</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kumar, Devinder</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of thermal analysis and calorimetry</subfield><subfield code="d">Springer Netherlands, 1998</subfield><subfield code="g">114(2013), 1 vom: 13. Jan., Seite 339-344</subfield><subfield code="w">(DE-627)244148767</subfield><subfield code="w">(DE-600)1429493-X</subfield><subfield code="w">(DE-576)066397693</subfield><subfield code="x">1388-6150</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:114</subfield><subfield code="g">year:2013</subfield><subfield code="g">number:1</subfield><subfield code="g">day:13</subfield><subfield code="g">month:01</subfield><subfield code="g">pages:339-344</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/s10973-012-2894-1</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">114</subfield><subfield code="j">2013</subfield><subfield code="e">1</subfield><subfield code="b">13</subfield><subfield code="c">01</subfield><subfield code="h">339-344</subfield></datafield></record></collection>
|
| score |
7.401 |