Hydrothermal syntheses and crystal structures of two new phosphomolybdates based on an organoamine template

Yan, Dan; Zheng, Lei; Zhang, Zhibin; Yuan, Yan; Zhu, Dunru; Xu, Yan

doi:10.1080/00958972.2010.534783

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Cited by 9 publications

(2 citation statements)

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“…In addition, broad bands at 3247-3440 cm À1 are due to ν(O-H) and ν (N-H). The features are in agreement with reported compounds [22,35,36].…”

Section: Infrared Spectrasupporting

confidence: 93%

Hydrothermal synthesis and structural characterization of three reduced phosphomolybdates

Yan

et al. 2013

Journal of Coordination Chemistry

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“…In addition, broad bands at 3247-3440 cm À1 are due to ν(O-H) and ν (N-H). The features are in agreement with reported compounds [22,35,36].…”

Section: Infrared Spectrasupporting

confidence: 93%

Hydrothermal synthesis and structural characterization of three reduced phosphomolybdates

Yan

et al. 2013

Journal of Coordination Chemistry

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“…Compounds 1 and 2 have been hydrothermally assembled by HIN and H 2 bdc [26]. As we all known, several factors such as initial reagents, pH values, temperature and reaction time can influence the growth of final crystals [27,28]. During our research, we find that the types of initial reagents were crucial in the synthesis.…”

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confidence: 96%

Hydrothermal synthesis, crystal structure and properties of two new coordination polymers structured by two mixed ligands and strict quadrangular {Ln3}8 Units (Ln=Er and Ho)

Chen

Huang

Deng

et al. 2012

Inorganic Chemistry Communications

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A Series of Lanthanide Metal–Organic Frameworks with Interesting Adjustable Photoluminescence Constructed by Helical Chains

Liu

Zhou

et al. 2015

Chemistry A European J

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Based on the isonicotinic acid (HIN=pyridine-4-carboxylic acid), seven lanthanide metal-organic frameworks (MOFs) with the formula [Ln(IN)2 L] (Ln=Eu (1), Tb (2), Er (3), Dy (4), Ho (5), Gd (6), La (7), L=OCH2 CH2 OH) have been synthesized by mixing Ln2 O3 with HIN under solvothermal conditions, and characterized by single-crystal X-ray diffraction, powder X-ray diffraction, infrared spectroscopy, and fluorescence spectroscopy. Crystal structural analysis shows that compounds 1-6 are isostructural, crystallize in a chiral space group P21 21 21 , whereas compound 7 crystallizes in space group C2/c. Nevertheless, they all consist of new intertwined chains. Simultaneously, on the basis of the above-mentioned compounds, we have realized a rational design strategy to form the doped Ln MOFs [(Eux Tb1-x )(IN)2 L] (x=0.35 (8), x=0.19 (9), x=0.06 (10)) by utilizing Tb(III) as the second "rare-earth metal". Interestingly, the photoluminescence of [(Eux Tb1-x )(IN)2 L] are not only adjustable by the ratios of Eu/Tb, but also temperature or excitation wavelength.

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Hydrothermal syntheses and crystal structures of two new phosphomolybdates based on an organoamine template

Abstract: 2010) Hydrothermal syntheses and crystal structures of two new phosphomolybdates based on an organoamine template, Journal of Coordination Chemistry, 63:24, 4215-4225,

Cited by 9 publications

References 41 publications

Hydrothermal synthesis and structural characterization of three reduced phosphomolybdates

Hydrothermal synthesis and structural characterization of three reduced phosphomolybdates

Hydrothermal synthesis, crystal structure and properties of two new coordination polymers structured by two mixed ligands and strict quadrangular {Ln3}8 Units (Ln=Er and Ho)

A Series of Lanthanide Metal–Organic Frameworks with Interesting Adjustable Photoluminescence Constructed by Helical Chains

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