Controlling Metal Ion Counter Diffusion in Confined Spaces for In Situ Growth of Mixed Metal MOF Membranes for Gas Separation

AbstractAn understanding of magma chamber dynamics relies on answering three important yet highly controversial questions: where, why, and how magma chambers crystallize and differentiate. Here we report on a new natural phenomenon—the undercut-embayed chamber floor in the Bushveld Complex—which allows us to address these questions. The undercut-embayed floor is produced by magmatic karstification (i.e. erosion by dissolution) of the underlying cumulates by replenishing magmas that form basal flows on the chamber floor. This results in a few metres thick three-dimensional framework of spatially interconnected erosional remnants that separate the floor cumulates from the overlying resident melt. The basal flow in this environment is effectively cooled through the floor, inducing heterogeneous nucleation and in situ growth against much of its three-dimensional framework. The solidification front thus propagates in multiple directions from the surfaces of erosional remnants. Fractional crystallization may occur within this environment by convective removal of a compositional boundary layer from in situ growing crystals and is remarkably efficient even in very confined spaces. We propose that the way magma crystallizes and differentiates in the undercut-embayed chamber floor is likely common for the evolution of many basaltic magma chambers.

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Epitaxial growth manner and structure of superconducting oxide films

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100173145 ◽

1990 ◽

Vol 48 (4) ◽

pp. 2-3

Author(s):

Yoshichika Bando ◽

Takahito Terashima ◽

Kenji Iijima ◽

Kazunuki Yamamoto ◽

Kazuto Hirata ◽

...

Keyword(s):

Ultrathin Films ◽

Film Surface ◽

High Energy ◽

Epitaxial Films ◽

Layer By Layer ◽

Initial Growth ◽

In Situ Growth ◽

High Quality ◽

Activated Reactive Evaporation

The high quality thin films of high-Tc superconducting oxide are necessary for elucidating the superconducting mechanism and for device application. The recent trend in the preparation of high-Tc films has been toward “in-situ” growth of the superconducting phase at relatively low temperatures. The purpose of “in-situ” growth is to attain surface smoothness suitable for fabricating film devices but also to obtain high quality film. We present the investigation on the initial growth manner of YBCO by in-situ reflective high energy electron diffraction (RHEED) technique and on the structural and superconducting properties of the resulting ultrathin films below 100Å. The epitaxial films have been grown on (100) plane of MgO and SrTiO, heated below 650°C by activated reactive evaporation. The in-situ RHEED observation and the intensity measurement was carried out during deposition of YBCO on the substrate at 650°C. The deposition rate was 0.8Å/s. Fig. 1 shows the RHEED patterns at every stage of deposition of YBCO on MgO(100). All the patterns exhibit the sharp streaks, indicating that the film surface is atomically smooth and the growth manner is layer-by-layer.

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In situ growth of SrTiO3 thin films prepared by AACVD from strontium and titanium oxide bisdipivaloylmethanates

Solid State Ionics ◽

10.1016/s0167-2738(97)00336-6 ◽

1997 ◽

Vol 101-103 (1-2) ◽

pp. 183-190 ◽

Cited By ~ 1

Author(s):

J Peña

Keyword(s):

Thin Films ◽

Titanium Oxide ◽

In Situ Growth

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Metastasis of colorectal carcinoma to kidney with in-situ growth pattern mimicking primary renal/urothelial neoplasm

10.26226/morressier.578f37fbd462b8028d890515 ◽

2016 ◽

Author(s):

Jiri Soukup

Keyword(s):

Colorectal Carcinoma ◽

Growth Pattern ◽

In Situ Growth ◽

Urothelial Neoplasm

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Lithium-mediated Ferration of Fluoroarenes

CHIMIA International Journal for Chemistry ◽

10.2533/chimia.2020.866 ◽

2020 ◽

Vol 74 (11) ◽

pp. 866-870

Author(s):

Lewis C. H. Maddock ◽

Alan Kennedy ◽

Eva Hevia

Keyword(s):

Hydrogen Atom ◽

Organometallic Chemistry ◽

Room Temperature ◽

Structural Elucidation ◽

Side Reactions ◽

Metal Base ◽

Lithium Amide ◽

Mixed Metal ◽

Important Challenge

While fluoroaryl fragments are ubiquitous in many pharmaceuticals, the deprotonation of fluoroarenes using organolithium bases constitutes an important challenge in polar organometallic chemistry. This has been widely attributed to the low stability of the in situ generated aryl lithium intermediates that even at –78 °C can undergo unwanted side reactions. Herein, pairing lithium amide LiHMDS (HMDS = N{SiMe3}2) with FeII(HMDS)2 enables the selective deprotonation at room temperature of pentafluorobenzene and 1,3,5-trifluorobenzene via the mixed-metal base [(dioxane)LiFe(HMDS)3] (1) (dioxane = 1,4-dioxane). Structural elucidation of the organometallic intermediates [(dioxane)Li(HMDS)2Fe(ArF)] (ArF = C6F5, 2; 1,3,5-F3-C6H2, 3) prior electrophilic interception demonstrates that these deprotonations are actually ferrations, with Fe occupying the position previously filled by a hydrogen atom. Notwithstanding, the presence of lithium is essential for the reactions to take place as Fe II (HMDS)2 on its own is completely inert towards the metallation of these substrates. Interestingly 2 and 3 are thermally stable and they do not undergo benzyne formation via LiF elimination.

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