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Sue E. Boyd

Researcher at Griffith University

Publications -  76
Citations -  2553

Sue E. Boyd is an academic researcher from Griffith University. The author has contributed to research in topics: Crystal structure & Hydrogen bond. The author has an hindex of 26, co-authored 76 publications receiving 2230 citations. Previous affiliations of Sue E. Boyd include University of Birmingham & California Institute of Technology.

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Roles of biochar in improving phosphorus availability in soils: a phosphate adsorbent and a source of available phosphorus.

TL;DR: In this paper, the amount of phosphorus (P) in nine types of biochar (one natural woody biochar and eight manufactured plant derived biochars) extractable by deionized water, 0.5 N NaHCO 3 (pH = 8.5) and 0.4 N H 2 SO 4, respectively, and P adsorption on single biochar or soil/biochar mixtures were examined to investigate the potential effect and role of bio char in improving P availability in soils.
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Simple Mechanical Molecular and Supramolecular Machines: Photochemical and Electrochemical Control of Switching Processes

TL;DR: In this article, photochemical control of a self-assembled supramolecular 1:1 pseudorotaxane (formed between a tetracationic cyclophane, namely the tetrachloride salt of cyclobis(paraquat-p-phenylene), and 1,5-bis[2-(2-(1-hydroxy)ethoxy)thoxy)ethoxide]naphthalene) has been achieved in aqueous solution.
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Effect of feedstock and pyrolysis temperature on properties of biochar governing end use efficacy

TL;DR: In this article, the authors evaluate how feedstock characteristics and temperature influence biochar evolution during pyrolysis and establish their relationships with biochar potential for soil amendments, using principal component and cluster analyses.
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Oligocatenanes Made to Order1

TL;DR: In this paper, the construction of catenanes, comprised of between two and seven interlocked rings, has been achieved, and two tris-1,5-naphtho-57-crown-15 macrocycles template the formation of cyclobis(paraquat-4,4‘-biphenylene) to give a [3]catenane, which acts as a template for the constructions of one and then another cyclecyclobis (para-p-phenylene), giving a [4]- and [5]
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Synthesis of Glycodendrimers by Modification of Poly(propylene imine) Dendrimers

TL;DR: Modifications of DAB-dendr-(NH2)x with biologically active carbohydrates affords a new and simple approach to high molecular weight compounds that may be considered as neoglycoconjugates with perfectly symmetrical structures and that offer much promise as multivalent ligands involved in carbohydrate-protein interactions.