Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16

Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powd...
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Gespeichert in:

Autor*in:	Heyward, Carla [verfasserIn] McMillen, Colin D. Kolis, Joseph

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2013transfer abstract

Schlagwörter:	Borosilicate Single crystal structure Borate–phosphate Hydrothermal Borate–carbonate

Umfang:	8

Übergeordnetes Werk:	Enthalten in: Numerical analysis of wind turbines blade in deep dynamic stall - Karbasian, Hamid Reza ELSEVIER, 2022, Orlando, Fla
Übergeordnetes Werk:	volume:203 ; year:2013 ; pages:166-173 ; extent:8

Links:	Volltext

DOI / URN:	10.1016/j.jssc.2013.04.022

Katalog-ID:	ELV022251103

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245	1	0	\|a Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16
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520			\|a Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework.
520			\|a Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework.
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650		7	\|a Hydrothermal \|2 Elsevier
650		7	\|a Borate–carbonate \|2 Elsevier
700	1		\|a McMillen, Colin D. \|4 oth
700	1		\|a Kolis, Joseph \|4 oth
773	0	8	\|i Enthalten in \|n Academic Press \|a Karbasian, Hamid Reza ELSEVIER \|t Numerical analysis of wind turbines blade in deep dynamic stall \|d 2022 \|g Orlando, Fla \|w (DE-627)ELV008417474
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matchkey_str	heywardcarlamcmillencolindkolisjoseph:2013----:yrtemlyteiadtutrlnlssfemxdxainoaeb1b64p4o6
hierarchy_sort_str	2013transfer abstract
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publishDate	2013
allfields	10.1016/j.jssc.2013.04.022 doi GBVA2013020000019.pica (DE-627)ELV022251103 (ELSEVIER)S0022-4596(13)00216-8 DE-627 ger DE-627 rakwb eng 540 540 DE-600 530 620 VZ 52.56 bkl Heyward, Carla verfasserin aut Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16 2013transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate Elsevier McMillen, Colin D. oth Kolis, Joseph oth Enthalten in Academic Press Karbasian, Hamid Reza ELSEVIER Numerical analysis of wind turbines blade in deep dynamic stall 2022 Orlando, Fla (DE-627)ELV008417474 volume:203 year:2013 pages:166-173 extent:8 https://doi.org/10.1016/j.jssc.2013.04.022 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 52.56 Regenerative Energieformen alternative Energieformen VZ AR 203 2013 166-173 8 045F 540
spelling	10.1016/j.jssc.2013.04.022 doi GBVA2013020000019.pica (DE-627)ELV022251103 (ELSEVIER)S0022-4596(13)00216-8 DE-627 ger DE-627 rakwb eng 540 540 DE-600 530 620 VZ 52.56 bkl Heyward, Carla verfasserin aut Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16 2013transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate Elsevier McMillen, Colin D. oth Kolis, Joseph oth Enthalten in Academic Press Karbasian, Hamid Reza ELSEVIER Numerical analysis of wind turbines blade in deep dynamic stall 2022 Orlando, Fla (DE-627)ELV008417474 volume:203 year:2013 pages:166-173 extent:8 https://doi.org/10.1016/j.jssc.2013.04.022 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 52.56 Regenerative Energieformen alternative Energieformen VZ AR 203 2013 166-173 8 045F 540
allfields_unstemmed	10.1016/j.jssc.2013.04.022 doi GBVA2013020000019.pica (DE-627)ELV022251103 (ELSEVIER)S0022-4596(13)00216-8 DE-627 ger DE-627 rakwb eng 540 540 DE-600 530 620 VZ 52.56 bkl Heyward, Carla verfasserin aut Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16 2013transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate Elsevier McMillen, Colin D. oth Kolis, Joseph oth Enthalten in Academic Press Karbasian, Hamid Reza ELSEVIER Numerical analysis of wind turbines blade in deep dynamic stall 2022 Orlando, Fla (DE-627)ELV008417474 volume:203 year:2013 pages:166-173 extent:8 https://doi.org/10.1016/j.jssc.2013.04.022 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 52.56 Regenerative Energieformen alternative Energieformen VZ AR 203 2013 166-173 8 045F 540
allfieldsGer	10.1016/j.jssc.2013.04.022 doi GBVA2013020000019.pica (DE-627)ELV022251103 (ELSEVIER)S0022-4596(13)00216-8 DE-627 ger DE-627 rakwb eng 540 540 DE-600 530 620 VZ 52.56 bkl Heyward, Carla verfasserin aut Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16 2013transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate Elsevier McMillen, Colin D. oth Kolis, Joseph oth Enthalten in Academic Press Karbasian, Hamid Reza ELSEVIER Numerical analysis of wind turbines blade in deep dynamic stall 2022 Orlando, Fla (DE-627)ELV008417474 volume:203 year:2013 pages:166-173 extent:8 https://doi.org/10.1016/j.jssc.2013.04.022 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 52.56 Regenerative Energieformen alternative Energieformen VZ AR 203 2013 166-173 8 045F 540
allfieldsSound	10.1016/j.jssc.2013.04.022 doi GBVA2013020000019.pica (DE-627)ELV022251103 (ELSEVIER)S0022-4596(13)00216-8 DE-627 ger DE-627 rakwb eng 540 540 DE-600 530 620 VZ 52.56 bkl Heyward, Carla verfasserin aut Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16 2013transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework. Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate Elsevier McMillen, Colin D. oth Kolis, Joseph oth Enthalten in Academic Press Karbasian, Hamid Reza ELSEVIER Numerical analysis of wind turbines blade in deep dynamic stall 2022 Orlando, Fla (DE-627)ELV008417474 volume:203 year:2013 pages:166-173 extent:8 https://doi.org/10.1016/j.jssc.2013.04.022 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 52.56 Regenerative Energieformen alternative Energieformen VZ AR 203 2013 166-173 8 045F 540
language	English
source	Enthalten in Numerical analysis of wind turbines blade in deep dynamic stall Orlando, Fla volume:203 year:2013 pages:166-173 extent:8
sourceStr	Enthalten in Numerical analysis of wind turbines blade in deep dynamic stall Orlando, Fla volume:203 year:2013 pages:166-173 extent:8
format_phy_str_mv	Article
bklname	Regenerative Energieformen alternative Energieformen
institution	findex.gbv.de
topic_facet	Borosilicate Single crystal structure Borate–phosphate Hydrothermal Borate–carbonate
dewey-raw	540
isfreeaccess_bool	false
container_title	Numerical analysis of wind turbines blade in deep dynamic stall
authorswithroles_txt_mv	Heyward, Carla @@aut@@ McMillen, Colin D. @@oth@@ Kolis, Joseph @@oth@@
publishDateDaySort_date	2013-01-01T00:00:00Z
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They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. 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author	Heyward, Carla
spellingShingle	Heyward, Carla ddc 540 ddc 530 bkl 52.56 Elsevier Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16
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topic_title	540 540 DE-600 530 620 VZ 52.56 bkl Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16 Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate Elsevier
topic	ddc 540 ddc 530 bkl 52.56 Elsevier Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate
topic_unstemmed	ddc 540 ddc 530 bkl 52.56 Elsevier Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate
topic_browse	ddc 540 ddc 530 bkl 52.56 Elsevier Borosilicate Elsevier Single crystal structure Elsevier Borate–phosphate Elsevier Hydrothermal Elsevier Borate–carbonate
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hierarchy_parent_title	Numerical analysis of wind turbines blade in deep dynamic stall
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title	Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16
ctrlnum	(DE-627)ELV022251103 (ELSEVIER)S0022-4596(13)00216-8
title_full	Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16
author_sort	Heyward, Carla
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doi_str_mv	10.1016/j.jssc.2013.04.022
dewey-full	540 530 620
title_sort	hydrothermal synthesis and structural analysis of new mixed oxyanion borates: ba11b26o44(po4)2(oh)6, li9bab15o27(co3) and ba3si2b6o16
title_auth	Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16
abstract	Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework.
abstractGer	Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework.
abstract_unstemmed	Several new borate compounds, Ba11B26O44(PO4)2(OH)6 (1), Li9BaB15O27(CO3) (2), and Ba3Si2B6O16 (3) were synthesized containing other hetero-oxyanion building blocks in addition to the borate frameworks. They were all prepared under hydrothermal conditions and characterized by single crystal and powder X-ray diffraction, and IR spectroscopy. Crystal data: For 1; space group P2 1 /c, a=6.8909 (14)Å, b=13.629 (3)Å, c=25.851 (5)Å, β=90.04 (3)°; For 2; space group P-31c, a=8.8599 (13)Å, c=15.148 (3)Å; For 3; space group P-1, a=5.0414 (10)Å, b=7.5602 (15)Å, c=8.5374 (17)Å, α=77.15 (3)°, β=77.84 (3)°, γ=87.41 (3)° for 3. Compounds 1 and 2 contain isolated oxyanions [PO4]3− and [CO3]2− respectively, sitting in channels created by the borate framework, while structure 3 has the [SiO4]4− groups directly bonded to the borate groups creating a B–O–Si framework.
collection_details	GBV_USEFLAG_U GBV_ELV SYSFLAG_U
title_short	Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16
url	https://doi.org/10.1016/j.jssc.2013.04.022
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author2	McMillen, Colin D. Kolis, Joseph
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up_date	2024-07-06T21:32:09.577Z
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Hydrothermal synthesis and structural analysis of new mixed oxyanion borates: Ba11B26O44(PO4)2(OH)6, Li9BaB15O27(CO3) and Ba3Si2B6O16

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