All Stories

  1. End-functional polyolefins for block copolymer synthesis
  2. Molecules that reduce cancer cell metastasis and destroy cancer stem cells
  3. Mirror-Image Dependence: Targeting Enantiomeric G-Quadruplex DNA Using Triplex Metallohelices
  4. Polyolefin–Polar Block Copolymers from Versatile New Macromonomers
  5. Stereochemistry and amyloid inhibition: Asymmetric triplex metallohelices enantioselectively bind to Aβ peptide
  6. Antifreeze Protein Mimetic Metallohelices with Potent Ice Recrystallization Inhibition Activity
  7. Chiral metallohelices enantioselectively target hybrid human telomeric G-quadruplex DNA
  8. Antimicrobial Metallodrugs
  9. Anticancer metallohelices: nanomolar potency and high selectivity
  10. Iron and Manganese Complexes of 2-Carbonyl Pyrrolyls: Scorpionate Sandwich Anions and Extended Structures
  11. Shape-selective recognition of DNA abasic sites by metallohelices: inhibition of human AP endonuclease 1
  12. All about the arrow
  13. Metallohelices: potential mimetics of α-helical peptides in cancer treatment?
  14. Single Molecule Microscopy and Properties of Olympicene: Olympic Rings at the molecular level
  15. Chiral Metallohelical Complexes Enantioselectively Target Amyloid β for Treating Alzheimer’s Disease
  16. Asymmetric triplex metallohelices with high and selective activity against cancer cells
  17. Metallohelices with activity against cisplatin-resistant cancer cells; does the mechanism involve DNA binding?
  18. Optically pure heterobimetallic helicates from self-assembly and click strategies
  19. Considerations of Noise and Measurement Reproducibility of Circular Dichroism Measurements Using Na[CoIII(EDDS)]
  20. Jahn–Teller effects on π-stacking and stereoselectivity in the phenylethaniminopyridine tris-chelates Cu(NN′)32+
  21. Optically pure, water-stable metallo-helical ‘flexicate’ assemblies with antibiotic activity
  22. Structural and Electronic Modulation of Magnetic Properties in a Family of Chiral Iron Coordination Polymers
  23. Chiral Semiconductor Phases: The Optically Pure D3[MIII(S,S-EDDS)]2 (D = TTF, TSF) Family
  24. Zirconium-Catalyzed Polymerization of a Styrene: Catalyst Reactivation Mechanisms Using Alkenes and Dihydrogen
  25. Isomeric Fe(ii) MOFs: from a diamond-framework spin-crossover material to a 2D hard magnet
  26. Dalton Transactions after 40 volumes
  27. Approaches to the synthesis of optically pure helicates
  28. Explanation of an unusually high selectivity in synthesis of metal-ligand complexes
  29. d0 organometallics in catalysis
  30. Comments on “Synthesis and characterisation of enantiopure copper(ii) complexes with chiral bidentate ligands”
  31. TTF salts of optically pure cobalt pyridine amidates; detection of soluble assemblies with stoichiometry corresponding to the solid state
  32. Mechanism of Catalytic Cyclohydroamination by Zirconium Salicyloxazoline Complexes
  33. fac-Specific syntheses of homochiral [Fe(NN′)3]2+ complexes (NN′ = pyridine keto-hydrazone); origins of the stereoselectivity
  34. Organic-soluble optically pure anionic metal complexes PPh4[MIII(S,S-EDDS)]·2H2O (M = Fe, Co, Cr)
  35. Chirality and diastereoselection in the μ-oxo diiron complexes L2Fe–O–FeL2 (L = bidentate salicylaldiminato)
  36. Dalton Discussion 12: Catalytic C–H and C–X bond activation (DD12)
  37. Substituent effects in ethene/styrene copolymerization: Dormant state destabilization?
  38. Self-assembling optically pure Fe(A–B)3 chelates
  39. A new reference material for UV-visible circular dichroism spectroscopy
  40. Single Diastereomer Half-Sandwich Salicyloxazoline Complexes of Titanium and Zirconium
  41. Awakening a dormant catalyst: salicylaldimine systems for ethene/tert-butylstyrene copolymerization
  42. Constrained geometry aminooxazolinate ligands giving chiral zirconium guanidinates; catalytic cyclohydroamination
  43. Catalytic alkene cyclohydroamination via an imido mechanism
  44. Chiral Alkoxide-Functionalized Guanidinates from Ring-Opening Rearrangement of Aminooxazolinate Complexes
  45. Half-Sandwich Group 4 Salicyloxazoline Catalysts
  46. Expression of chirality in salicyloxazolinate complexes of zirconium
  47. Group 4 catalysts for ethene polymerization containing tetradentate salicylaldiminato ligands
  48. Group 4 salicyloxazolines are potent polymerization catalysts
  49. Chiral Complexes of a New Diazaallyl Ligand:  Group 4 Aminooxazolinates
  50. Chiral biarylamido/anisole complexes of yttrium in enantioselective aminoalkene hydaroamination/cyclisation
  51. Zirconium catalysed enantioselective hydroamination/cyclisationElectronic Supplementary Information (ESI) available: experimental details and characterising data for complexes and substrates, catalytic protocol, determination of ee, crystal data for [Z...
  52. Chiral metal architectures in aminopyridinato complexes of zirconium
  53. Aminooxazolinate; a chiral amidinate analogue
  54. Arylaminopyridinato complexes of zirconiumElectronic supplementary information (ESI) available: Rotatable 3-D crystal structure diagrams and NMR spectra. See
  55. Biaryl amine ligands for lanthanide catalysed enantioselective hydroamination/cyclisation of aminoalkenes
  56. Chiral Titanium Bis(aminopyridinates) Based on a Biaryl Backbone
  57. Predetermination of chirality at octahedral centres with tetradentate ligands: prospects for enantioselective catalysis
  58. Non-planar manganese Schiff-base complexes; synthesis and molecular structures
  59. Chiral-at-metal organolanthanides: enantioselective aminoalkene hydroamination/cyclisation with non-cyclopentadienylsElectronic supplementary information (ESI) available: complete experimental procedures and characterising data for all ligands and comp...
  60. Chiral Biarylamido Complexes of Zirconium
  61. Enantioselective Aziridination Using Copper Complexes of Biaryl Schiff Bases
  62. Reactivity of a triamidoamine complex of trivalent uranium
  63. Efficient predetermination of chirality-at-zirconium
  64. Structural Origins of a Dramatic Variation in Catalyst Efficiency in Enantioselective Alkene Aziridination:  Implications for Design of Ligands Based on Chiral Biaryldiamines