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Alexander J. Blake

Researcher at University of Nottingham

Publications -  1136
Citations -  37892

Alexander J. Blake is an academic researcher from University of Nottingham. The author has contributed to research in topics: Crystal structure & Ligand. The author has an hindex of 89, co-authored 1133 publications receiving 35746 citations. Previous affiliations of Alexander J. Blake include University of Illinois at Chicago & University of Wisconsin-Madison.

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Platinum thioether macrocyclic chemistry: synthesis and electrochemistry of [PtL][PF6]2(L =[12]-, [14]- or [16]-aneS4) and [Pt2([28]aneS8)][PF6]4. Crystal structure of [Pt([12]aneS4)][PF6]2·MeCN

TL;DR: A series of mono-and bi-nuclear platinum(II) complexes [PtL][PF6]2(L =[12]-, [14]- or [16]-aneS4) and [PT2([28]aneS8)][PF 6]4 have been synthesised by reaction of the crown thioethers with platinum (II) salts.
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Supramolecular isomers of metal-organic frameworks: the role of a new mixed donor imidazolate-carboxylate tetradentate ligand.

TL;DR: Five new metal-organic frameworks prepared from the ligand 5-bis(3-(1-imidazolyl)propylcarbamoyl)terephthalate and transition metal salts are reported, revealing that the bipta(2-) ligand acts as a tetradentate ligand and combines with four-coordinate cationic metal nodes to give four-connected framework structures.
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Two approaches to the aromatic core of the aminonaphthoquinone antibiotics.

TL;DR: Two complementary approaches are presented for the synthesis of the quinone chromophores of the naphthoquinone ansamycins and related natural products using an improved protocol for the manganese(III) acetate mediated cyclization of 5-aryl-1,3-dicarbonyl compounds to β-naphthols.
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Synthesis and Characterisation of Lanthanide N-Trimethylsilyl and -Mesityl Functionalised Bis(iminophosphorano)methanides and -Methanediides

TL;DR: In this article, the authors report the extension of the series of {BIPMTMSH}− (BIPMR = C{PPh2NR}2, TMS = trimethylsilyl) derived rare earth methanides by the preparation of [Ln(BIPMMesH)(I)2(THF)] (Ln = Nd, Gd, Tb), 1a-c, in 34-50% crystalline yields via the reaction of [ln(I)3 (THF)3.5
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Synthesis, structure and redox properties of bis(cyclopentadienyl)dithiolene complexes of molybdenum and tungsten

TL;DR: Results have been interpreted successfully within the framework provided by DFT calculations and the EPR spectra of each of the Mo cations show that the unpaired electron is coupled to the dithiolene proton but relatively weakly to (95,97)Mo.