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Synthesis and Characterization of Inorganic-Organic Derivatives of Layered Perovskite-like Niobate HSr2Nb3O10 with n-Amines and n-Alcohols. / Khramova, A.D.; Silyukov, O.I.; Kurnosenko, S.A.; Malygina, E.N.; Zvereva, I.A.

In: Molecules, Vol. 28, No. 12, 4807, 16.06.2023.

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@article{8d4e72b11ce54940a6dd3b1987bd66c3,
title = "Synthesis and Characterization of Inorganic-Organic Derivatives of Layered Perovskite-like Niobate HSr2Nb3O10 with n-Amines and n-Alcohols",
abstract = "A protonated and hydrated Dion-Jacobson-phase HSr 2Nb 3O 10∙yH 2O was used to prepare two series of inorganic-organic derivatives containing non-covalently intercalated n-alkylamines and covalently grafted n-alkoxy groups of different lengths, as they are promising hybrid materials for photocatalytic applications. Preparation of the derivatives was carried out both under the conditions of standard laboratory synthesis and by solvothermal methods. For all the hybrid compounds synthesized structure, quantitative composition, a type of bonding between inorganic and organic parts as well as light absorption range were discussed using powder XRD, Raman, IR and NMR spectroscopy, TG, elemental CHN analysis, and DRS. It was shown that the inorganic-organic samples obtained contain approximately one interlayer organic molecule or group per proton of the initial niobate, as well as some amount of intercalated water. In addition, the thermal stability of the hybrid compounds strongly depends on the nature of the organic component anchoring to the niobate matrix. Although non-covalent amine derivatives are stable only at low temperatures, covalent alkoxy ones can withstand heat up to 250 °C without perceptible decomposition. The fundamental absorption edge of both the initial niobate and the products of its organic modification lies in the near-ultraviolet region (370-385 nm). ",
keywords = "слоистые соединения; перовскит; ниобат; органо-неорганический гибрид; интеркаляция; графтинг, layered compounds; perovskite; niobate; inorganic-organic hybrid; intercalation; grafting",
author = "A.D. Khramova and O.I. Silyukov and S.A. Kurnosenko and E.N. Malygina and I.A. Zvereva",
note = "Khramova, A.D.; Silyukov, O.I.; Kurnosenko, S.A.; Malygina, E.N.; Zvereva, I.A. Synthesis and Characterization of Inorganic- Organic Derivatives of Layered Perovskite-like Niobate HSr2Nb3O10 with n-Amines and n-Alcohols. Molecules 2023, 28, 4807",
year = "2023",
month = jun,
day = "16",
doi = "10.3390/molecules28124807",
language = "English",
volume = "28",
journal = "Molecules",
issn = "1420-3049",
publisher = "MDPI AG",
number = "12",

}

RIS

TY - JOUR

T1 - Synthesis and Characterization of Inorganic-Organic Derivatives of Layered Perovskite-like Niobate HSr2Nb3O10 with n-Amines and n-Alcohols

AU - Khramova, A.D.

AU - Silyukov, O.I.

AU - Kurnosenko, S.A.

AU - Malygina, E.N.

AU - Zvereva, I.A.

N1 - Khramova, A.D.; Silyukov, O.I.; Kurnosenko, S.A.; Malygina, E.N.; Zvereva, I.A. Synthesis and Characterization of Inorganic- Organic Derivatives of Layered Perovskite-like Niobate HSr2Nb3O10 with n-Amines and n-Alcohols. Molecules 2023, 28, 4807

PY - 2023/6/16

Y1 - 2023/6/16

N2 - A protonated and hydrated Dion-Jacobson-phase HSr 2Nb 3O 10∙yH 2O was used to prepare two series of inorganic-organic derivatives containing non-covalently intercalated n-alkylamines and covalently grafted n-alkoxy groups of different lengths, as they are promising hybrid materials for photocatalytic applications. Preparation of the derivatives was carried out both under the conditions of standard laboratory synthesis and by solvothermal methods. For all the hybrid compounds synthesized structure, quantitative composition, a type of bonding between inorganic and organic parts as well as light absorption range were discussed using powder XRD, Raman, IR and NMR spectroscopy, TG, elemental CHN analysis, and DRS. It was shown that the inorganic-organic samples obtained contain approximately one interlayer organic molecule or group per proton of the initial niobate, as well as some amount of intercalated water. In addition, the thermal stability of the hybrid compounds strongly depends on the nature of the organic component anchoring to the niobate matrix. Although non-covalent amine derivatives are stable only at low temperatures, covalent alkoxy ones can withstand heat up to 250 °C without perceptible decomposition. The fundamental absorption edge of both the initial niobate and the products of its organic modification lies in the near-ultraviolet region (370-385 nm).

AB - A protonated and hydrated Dion-Jacobson-phase HSr 2Nb 3O 10∙yH 2O was used to prepare two series of inorganic-organic derivatives containing non-covalently intercalated n-alkylamines and covalently grafted n-alkoxy groups of different lengths, as they are promising hybrid materials for photocatalytic applications. Preparation of the derivatives was carried out both under the conditions of standard laboratory synthesis and by solvothermal methods. For all the hybrid compounds synthesized structure, quantitative composition, a type of bonding between inorganic and organic parts as well as light absorption range were discussed using powder XRD, Raman, IR and NMR spectroscopy, TG, elemental CHN analysis, and DRS. It was shown that the inorganic-organic samples obtained contain approximately one interlayer organic molecule or group per proton of the initial niobate, as well as some amount of intercalated water. In addition, the thermal stability of the hybrid compounds strongly depends on the nature of the organic component anchoring to the niobate matrix. Although non-covalent amine derivatives are stable only at low temperatures, covalent alkoxy ones can withstand heat up to 250 °C without perceptible decomposition. The fundamental absorption edge of both the initial niobate and the products of its organic modification lies in the near-ultraviolet region (370-385 nm).

KW - слоистые соединения; перовскит; ниобат; органо-неорганический гибрид; интеркаляция; графтинг

KW - layered compounds; perovskite; niobate; inorganic-organic hybrid; intercalation; grafting

UR - https://www.mendeley.com/catalogue/34f375a2-f06d-372b-8ab4-c9c310843dd8/

U2 - 10.3390/molecules28124807

DO - 10.3390/molecules28124807

M3 - Article

C2 - 37375362

VL - 28

JO - Molecules

JF - Molecules

SN - 1420-3049

IS - 12

M1 - 4807

ER -

ID: 106662923