Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data
High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4,...
Ausführliche Beschreibung
Autor*in: |
Martucci, Annalisa [verfasserIn] Gigli, Lara [verfasserIn] Plaisier, Jasper Rikkert [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2020 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Microporous and mesoporous materials - Amsterdam [u.a.] : Elsevier, 1998, 307 |
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Übergeordnetes Werk: |
volume:307 |
DOI / URN: |
10.1016/j.micromeso.2020.110505 |
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Katalog-ID: |
ELV004634969 |
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100 | 1 | |a Martucci, Annalisa |e verfasserin |0 (orcid)0000-0002-6467-881X |4 aut | |
245 | 1 | 0 | |a Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data |
264 | 1 | |c 2020 | |
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520 | |a High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. | ||
650 | 4 | |a 6-Azonia-spiro-[5,5]-undecane | |
650 | 4 | |a ZSM-12 | |
650 | 4 | |a X-ray synchrotron powder diffraction data | |
650 | 4 | |a SDA conformation | |
650 | 4 | |a Rietveld refinement | |
700 | 1 | |a Gigli, Lara |e verfasserin |4 aut | |
700 | 1 | |a Plaisier, Jasper Rikkert |e verfasserin |0 (orcid)0000-0003-1981-1498 |4 aut | |
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10.1016/j.micromeso.2020.110505 doi (DE-627)ELV004634969 (ELSEVIER)S1387-1811(20)30507-2 DE-627 ger DE-627 rda eng 530 DE-600 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 bkl Martucci, Annalisa verfasserin (orcid)0000-0002-6467-881X aut Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. 6-Azonia-spiro-[5,5]-undecane ZSM-12 X-ray synchrotron powder diffraction data SDA conformation Rietveld refinement Gigli, Lara verfasserin aut Plaisier, Jasper Rikkert verfasserin (orcid)0000-0003-1981-1498 aut Enthalten in Microporous and mesoporous materials Amsterdam [u.a.] : Elsevier, 1998 307 Online-Ressource (DE-627)318368277 (DE-600)2012505-7 (DE-576)09529998X 1387-1811 nnns volume:307 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 38.30 Mineralogie 35.68 Organische Verbindungen: Sonstiges 33.61 Festkörperphysik 35.90 Festkörperchemie 51.45 Werkstoffe mit besonderen Eigenschaften AR 307 |
spelling |
10.1016/j.micromeso.2020.110505 doi (DE-627)ELV004634969 (ELSEVIER)S1387-1811(20)30507-2 DE-627 ger DE-627 rda eng 530 DE-600 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 bkl Martucci, Annalisa verfasserin (orcid)0000-0002-6467-881X aut Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. 6-Azonia-spiro-[5,5]-undecane ZSM-12 X-ray synchrotron powder diffraction data SDA conformation Rietveld refinement Gigli, Lara verfasserin aut Plaisier, Jasper Rikkert verfasserin (orcid)0000-0003-1981-1498 aut Enthalten in Microporous and mesoporous materials Amsterdam [u.a.] : Elsevier, 1998 307 Online-Ressource (DE-627)318368277 (DE-600)2012505-7 (DE-576)09529998X 1387-1811 nnns volume:307 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 38.30 Mineralogie 35.68 Organische Verbindungen: Sonstiges 33.61 Festkörperphysik 35.90 Festkörperchemie 51.45 Werkstoffe mit besonderen Eigenschaften AR 307 |
allfields_unstemmed |
10.1016/j.micromeso.2020.110505 doi (DE-627)ELV004634969 (ELSEVIER)S1387-1811(20)30507-2 DE-627 ger DE-627 rda eng 530 DE-600 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 bkl Martucci, Annalisa verfasserin (orcid)0000-0002-6467-881X aut Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. 6-Azonia-spiro-[5,5]-undecane ZSM-12 X-ray synchrotron powder diffraction data SDA conformation Rietveld refinement Gigli, Lara verfasserin aut Plaisier, Jasper Rikkert verfasserin (orcid)0000-0003-1981-1498 aut Enthalten in Microporous and mesoporous materials Amsterdam [u.a.] : Elsevier, 1998 307 Online-Ressource (DE-627)318368277 (DE-600)2012505-7 (DE-576)09529998X 1387-1811 nnns volume:307 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 38.30 Mineralogie 35.68 Organische Verbindungen: Sonstiges 33.61 Festkörperphysik 35.90 Festkörperchemie 51.45 Werkstoffe mit besonderen Eigenschaften AR 307 |
allfieldsGer |
10.1016/j.micromeso.2020.110505 doi (DE-627)ELV004634969 (ELSEVIER)S1387-1811(20)30507-2 DE-627 ger DE-627 rda eng 530 DE-600 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 bkl Martucci, Annalisa verfasserin (orcid)0000-0002-6467-881X aut Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. 6-Azonia-spiro-[5,5]-undecane ZSM-12 X-ray synchrotron powder diffraction data SDA conformation Rietveld refinement Gigli, Lara verfasserin aut Plaisier, Jasper Rikkert verfasserin (orcid)0000-0003-1981-1498 aut Enthalten in Microporous and mesoporous materials Amsterdam [u.a.] : Elsevier, 1998 307 Online-Ressource (DE-627)318368277 (DE-600)2012505-7 (DE-576)09529998X 1387-1811 nnns volume:307 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 38.30 Mineralogie 35.68 Organische Verbindungen: Sonstiges 33.61 Festkörperphysik 35.90 Festkörperchemie 51.45 Werkstoffe mit besonderen Eigenschaften AR 307 |
allfieldsSound |
10.1016/j.micromeso.2020.110505 doi (DE-627)ELV004634969 (ELSEVIER)S1387-1811(20)30507-2 DE-627 ger DE-627 rda eng 530 DE-600 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 bkl Martucci, Annalisa verfasserin (orcid)0000-0002-6467-881X aut Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. 6-Azonia-spiro-[5,5]-undecane ZSM-12 X-ray synchrotron powder diffraction data SDA conformation Rietveld refinement Gigli, Lara verfasserin aut Plaisier, Jasper Rikkert verfasserin (orcid)0000-0003-1981-1498 aut Enthalten in Microporous and mesoporous materials Amsterdam [u.a.] : Elsevier, 1998 307 Online-Ressource (DE-627)318368277 (DE-600)2012505-7 (DE-576)09529998X 1387-1811 nnns volume:307 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 38.30 Mineralogie 35.68 Organische Verbindungen: Sonstiges 33.61 Festkörperphysik 35.90 Festkörperchemie 51.45 Werkstoffe mit besonderen Eigenschaften AR 307 |
language |
English |
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Enthalten in Microporous and mesoporous materials 307 volume:307 |
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Enthalten in Microporous and mesoporous materials 307 volume:307 |
format_phy_str_mv |
Article |
bklname |
Mineralogie Organische Verbindungen: Sonstiges Festkörperphysik Festkörperchemie Werkstoffe mit besonderen Eigenschaften |
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topic_facet |
6-Azonia-spiro-[5,5]-undecane ZSM-12 X-ray synchrotron powder diffraction data SDA conformation Rietveld refinement |
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Microporous and mesoporous materials |
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Martucci, Annalisa @@aut@@ Gigli, Lara @@aut@@ Plaisier, Jasper Rikkert @@aut@@ |
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2020-01-01T00:00:00Z |
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Martucci, Annalisa |
spellingShingle |
Martucci, Annalisa ddc 530 bkl 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 misc 6-Azonia-spiro-[5,5]-undecane misc ZSM-12 misc X-ray synchrotron powder diffraction data misc SDA conformation misc Rietveld refinement Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data |
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530 DE-600 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 bkl Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data 6-Azonia-spiro-[5,5]-undecane ZSM-12 X-ray synchrotron powder diffraction data SDA conformation Rietveld refinement |
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ddc 530 bkl 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 misc 6-Azonia-spiro-[5,5]-undecane misc ZSM-12 misc X-ray synchrotron powder diffraction data misc SDA conformation misc Rietveld refinement |
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ddc 530 bkl 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 misc 6-Azonia-spiro-[5,5]-undecane misc ZSM-12 misc X-ray synchrotron powder diffraction data misc SDA conformation misc Rietveld refinement |
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ddc 530 bkl 38.30 bkl 35.68 bkl 33.61 bkl 35.90 bkl 51.45 misc 6-Azonia-spiro-[5,5]-undecane misc ZSM-12 misc X-ray synchrotron powder diffraction data misc SDA conformation misc Rietveld refinement |
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Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data |
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Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data |
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Microporous and mesoporous materials |
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Martucci, Annalisa Gigli, Lara Plaisier, Jasper Rikkert |
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title_sort |
location of 6-azonia-spiro- [5,5]-undecane molecules in zsm-12 using x-ray synchrotron powder diffraction data |
title_auth |
Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data |
abstract |
High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. |
abstractGer |
High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. |
abstract_unstemmed |
High-silica ZSM-12 (MTW topology), synthesized with 6-azonia-spiro- (Rimer, 2018; Rimer, 2018) [5,5]-undecane as structure directing agent (SDA), was carefully characterized by using X-ray synchrotron powder diffraction. The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts. |
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title_short |
Location of 6-azonia-spiro- [5,5]-undecane molecules in ZSM-12 using X-ray synchrotron powder diffraction data |
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Gigli, Lara Plaisier, Jasper Rikkert |
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The structure refinement led to a monoclinic unit cell (space group Cc, Z = 4, a = 25.0814(13) Å, b = 15.0987(8) Å, c = 24.4419(17) Å, β = 107.844(6), V = 8810.8(8) Å3) with a three times enlargement of the unit cell along the b axis with respect to the calcined starting ZSM-12 (space group C2/c, Z = 1, a = 24.8633(3) Å, b = 5.01238(7) Å, c = 24.3275(7) Å, β = 107.7215(6)°). The SDAs conformation and position in the framework structure did not maintain the twofold axes coinciding with the crystallographic twofold axis thus changing the space group symmetry from C2/c to Cc. The structure refinement gave an extraframework content 6.13 SDA molecules per unit cell (corresponding to ~9.0 wt%) in good agreement with the weight loss given by the thermogravimetric analysis. The refined bond distances revealed the occurrence of non-bonding interactions of both azonia molecules with the MTW pore wall. AZO-1 and AZO-2 molecules are H-bonded between them thus forming clusters aligned along the b axis. This information is crucial to tailor the physicochemical properties of zeolites as well as to address their hydrophobicity, pore dimensions and cavities thus optimizing the selectivity of zeolite catalysts.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">6-Azonia-spiro-[5,5]-undecane</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ZSM-12</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">X-ray synchrotron powder diffraction data</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">SDA conformation</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Rietveld refinement</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gigli, Lara</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Plaisier, Jasper 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