Independent publications

2018:

51) A. Hakonen*, J. E. Beves
Hue Parameter Fluorescence Identification of Edible Oils with a Smartphone
ACS Sens., 2018, DOI: 10.1021/acssensors.8b00409

Oils

50) N. Mallo, E. D. Foley, H. Iranmanesh, A. D. W. Kennedy, E. T. Luis, J. Ho, J. B. Harper, J. E. Beves*
Structure–function relationships of donor–acceptor Stenhouse adduct photochromic switches
Chem. Sci. 2018, DOI: 10.1039/C8SC03218A

GA-TOC

49) E. T. Luis, H. Iranmanesh, K. S. A. Arachchige, W. A. Donald, G. Quach, E. G. Moore, J. E. Beves*
Luminescent Tetrahedral Molecular Cages Containing Ruthenium(II) Chromophores
Inorg. Chem., 2018, 57, 8476–8486.

graphical-abstract

 

48) J. N. Bull, E. Carrascosa, N. Mallo, M. S. Scholz, G. da Silva, J. E. Beves, E. J. Bieske*
Photoswitching An Isolated Donor–Acceptor Stenhouse Adduct
J. Phys. Chem. Lett.20189, 665–671.

jz-2017-03402v_0006

2017:

47) S. V. F. Beddoe, A. J. Fitzpatrick, J. R. Price, N. Mallo, J. E. Beves, G. G. Morgan, J. A. Kitchen and T. D. Keene*
A Bridge Too Far: Testing the Limits of Polypyridyl Ligands in Bridging Soluble Subunits of a Coordination Polymer
Cryst. Grow. Des., 2017, 17, 6603–6612.

A_bridge_too_far

46) Y. Zhao, V. Mandadapu, H. Iranmanesh, J. E. Beves and A. I. Day*
The Inheritance Angle: A Determinant for the Number of Members in the Substituted Cucurbit[n]uril Family
Org. Lett., 2017, 19, 4034-4037.

Q_inherit

45) S. Chao, A. D. W. Kennedy, W. A. Donald, A. M. Torres, W. S. Price, J. E. Beves*
Self-assembled supramolecular cages containing dinuclear ruthenium(II) polypyridyl complexes
Inorg. Chim. Acta, 2017, 458, 122-128
aaron-cage-for-web_even_smaller44) H. Iranmanesh, K. S. A. Arachchige, W. A. Donald, N. Kyriacou, C. Shen, J. R. Price, J. E. Beves*
Rage against conformity: ruthenium(II) bisterpyridine complexes respond to crystal engineering instructions with whelming results
Aust. J. Chem., 2017, 70, 529-537

fig-for-web

2016:

43) H. Iranmanesh, K. S. A. Arachchige, M. Bhadbhade, W. A. Donald, K. T.-C. Liu, E. T. Luis, E. G. Moore,* J. Y. Liew, J. R. Price, H. Yan, J. Yang, J. E. Beves*
Chiral Ruthenium(II) Complexes as Supramolecular Building Blocks for Heterometallic Self-Assembly
Inorg. Chem., 2016, 55, 12737−12751
hasti_ic_toc

42) N. Mallo, P. T. Brown, H. Iranmanesh, T. S. C. MacDonald, M. J. Teusner, J. B. Harper, G. E. Ball, J. E. Beves*
Photochromic Switching Behaviour of Donor-Acceptor Stenhouse Adducts in Organic Solvents
Chem. Commun., 2016, 52, 13576-13579

dasa_tocphoto_nmr_for_web

41) E. T. Luis, G. E. Ball, A. Gilbert, H. Iranmanesh, C. W. Newdick, J. E. Beves*
Efficient microwave-assisted synthesis and characterization of key ruthenium(II) polypyridyl complexes [Ru(bpy)3](PF6)2, [Ru(phen)3](PF6)2, [Ru(bpy)2)(phen)](PF6)2 and [Ru(phen)2(bpy)](PF6)2
J. Coord. Chem., 2016, 69, 1686-1694.ga_web

40) Fei-Long Hu, Hui-Fang Wang, Dong Guo, Hui Zhang, Jian-the Ping Lang, J. E. Beves*
Controlled Formation of Chiral Networks, and Their Reversible Chiroptical Switching Behavior by the UV / Microwave Irradiation
Chem. Commun. , 2016 , 52, 7990-7993.
mof_toc39) C. Shen, P. Wang, J. E. Beves*
New Ruthenium (II) Complexes of 2,2′:6′,2”-terpyridine Derivatives as Supramolecular Building Blocks.
Polyhedron, 2016 , 103 , 241 -247.

2015:

38) H. Iranmanesh, M. Bhadbhade, N. De Haas, E. T. Luis, H. Yan, J. Yang, J. E. Beves*
Badly behaving bipyridine: The surprising coordination behaviour of 5,5’-substituted-2,2’-bipyridine towards iron(II) and ruthenium(II) ions.
Supramol. Chem., 2015, 27, 854-864
graphical-abstract

 

37) J. Yang, M. Bhadbhade, W. A. Donald, H. Iranmanesh, E. G. Moore, H. Yan and J. E. Beves*
Self-assembled supramolecular cages containing ruthenium(II) polypyridyl complexes
Chem. Commun., 2015, 51, 4465 – 4468
graphical-abstract

2014:

36) A. Hakonen, J. E. Beves, N. Strömberg
Digital colour tone for fluorescence sensing: A direct comparison of intensity, ratiometric and Hue based quantification
Analyst, 2014, 139, 3524-3527

2013:

35) J. Yang, J. K. Clegg, Q. Jiang, X. Lui, H. Yan, W. Zhong, J. E. Beves*
Multi-pyridine decorated Fe(II) and Ru(II) complexes by Pd(0)-catalysed cross couplings: new building blocks for metallosupramolecular assemblies
Dalton Trans. 2013, 42, 15625-15636
dalton_toc

34) Y.-Y. Li, F. Gao, J. E. Beves, Y.-Z. Li, J.-L. Zuo
A giant metallo-supramolecular cage encapsulating a single-molecule magnet
Chem. Commun. 2013, 3658-3660

Get

 

33) J. Xiong, L. Cui, W. Liu, J. E. Beves, Y. -Y.Li, J. -L. Zuo
Large and Selective Electrochemical Response to Fluoride by a Tetrathiafulvalene-Based Sensor
Tetrahedron Lett., 2013, 54, 1998-2000

Sensor.jpg

Post-doctoral work

2015:

32) J.-F. Ayme, J. E. Beves, C. J. Campbell, G. Gil-Ramírez, D. A. Leigh, A. J. Stephens,
Strong and Selective Anion Binding within the Central Cavity of Molecular Knots and Links
J. Am. Chem. Soc., 2015, 137, 812-9815.

31) J. E. Beves, J. J. Danon, D. A. Leigh, J.-F. Lemonnier, I. J. Vitorica-Yrezabal,
A Solomon Link through an Interwoven Molecular Grid
Angew. Chem., Int. Ed., 2015, 54, 7555-7559.

2014:

30) J.-F. Ayme, J. E. Beves, C. J. Campbell and D. A. Leigh,
The Self-Sorting Behavior of Circular Helicates and Molecular Knots and Links
Angew. Chem., Int. Ed., 2014, 53, 7823-7827.

29) J. E. Beves, V. Blanco, B. A. Blight, R. Carrillo, D. M. D’Souza; D. Howgego, D. A. Leigh, A. M. Z. Slawin, M. Symes,
Toward Metal Complexes that can Directionally Walk Along Tracks: Controlled Stepping of a Molecular Biped with a Palladium(II) Foot
J. Am. Chem. Soc., 2014, 136, 2094–2100.

2013:

28) J.-F. Ayme, J. E. Beves, C. J. Campbell, D. A. Leigh
Template Synthesis of Molecular Knots
Chem. Soc. Rev., 2013, 1700-1712.

27) J. E. Beves, C. J. Campbell, D. A. Leigh, R. Robin G. Pritchard
Tetrameric Cyclic Double Helicates as a Scaffold for a Molecular Solomon Link
Angew. Chem. Int. Ed., 2013, 52, 6464-6467.

2012:

26) J.-F. Ayme, J. E. Beves, D. A. Leigh, R. T. McBurney, D. Schultz
Pentameric Circular Iron(II) Double Helicates and a Molecular Pentafoil Knot
J. Am. Chem. Soc., 2012, 134, 9488-9497.

25) J. E. Beves*
Metal Template Synthesis of Molecular Knots and Links
Chimia, 2012, 66, 170-173.

24) J.-F. Ayme, J. E. Beves, D. A. Leigh, R. T. McBurney, D. Schultz
A molecular pentafoil knot
Nature Chem., 2012, 4, 15. (Front cover)

2011:

23) J. E. Beves, B. A. Blight, D. A. Leigh, R. T. McBurney
Strategies and tactics for the metal-template synthesis of catenanes, rotaxanes, knots and links
Angew. Chem. Int. Ed., 2011, 50, 9260-9327.

2010:

22) J. E. Beves, D. A. Leigh
Linking rings without templates
Nature Chem. (N&V) 2010, 2, 708.

PhD work

2009:

21) J. E. Beves, E. C. Constable, S. Decurtins, C. E. Housecroft, T. D. Keene, M. Neuburger, S. Schaffner, J. Zampese
Structural diversity in the reactions of 4′-(pyridyl)-2,2′:6′,2″-terpyridine ligands and bis{4′-(4-pyridyl)-2,2′:6′,2″-terpyridine}iron(II) with copper(II)
CrystEngComm, 2009, 2406.  

20) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner, J. A. Zampese
Building functionality into 4′-hydrazone derivatives of 2,2′:6′,2”-terpyridine
Helv. Chim. Acta, 2009, 92, 2214.

19) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner, J. A. Zampese
Substituent effects in homoleptic iron(II) and ruthenium(II) complexes of 4′-hydrazone derivatives of 2,2′:6′,2″-terpyridine
Polyhedron, 2009, 3828.

18) J. E. Beves, E. C. Constable, C. E. Housecroft; M. Neuburger, S. Schaffner
Ditopic, flexible hydrazone-based building blocks with pendant 2,2′:6′,2”-terpyridine metal-binding domains
Inorg. Chem. Commun., 2009, 12, 898. [IF = 1.762]

17) S. Silvi, E. C. Constable, C. E. Housecroft, J. E. Beves, E. L. Dunphy, M. Tomasulo, F. M. Raymo, A. Credi
Photochemical switching of luminescence and singlet oxygen generation by chemical signal communication
Chem. Commun., 2009, 1484.

16) S. Silvi, E. C. Constable, C. E. Housecroft, J. E. Beves, E. L. Dunphy, M. Tomasulo, F. M. Raymo, A. Credi,
All-optical integrated logic operations based on chemical communication between molecular switches
Chem.- Eur. J., 2009, 15, 178

2008:

15) J. E. Beves, E. C. Constable, C. E. Housecroft, C. J. Kepert, M. Neuburger, D. J. Price, S. Schaffner
Curly-curly, loop-loop: homoleptic metal(II) complexes of pyridinecarbaldehyde 4′-(2,2′:6′,2″-terpyridyl)hydrazones and their coordination polymers
Dalton Trans., 2008, 6742.

14) J. E. Beves, P. A. Chwalisz, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Silvia Schaffner, J. A. Zampese
A new polymorph of 4’-tolyl-2,2’:6’,2’’-terpyridine (ttpy) and the single crystal structures of Fe(ttpy)2](PF6)2 and [Ru(ttpy)2](PF6)2
Inorg. Chem. Commun., 2008, 11, 1009.

13) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Silvia Schaffner, J. A. Zampese
4’-Chloro-2,2’:6’,2’’-terpyridine (L): ethyl sulfate salt of [H2L]2+ and the single crystal structures of [H2L][EtOSO3]Cl.H2O and [ML2][PF6]2 with M = Fe and Ru.
Inorg. Chem. Commun., 2008, 11, 1006.

12) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner, J. A. Zampese
4’-Hydrazone derivatives of 2, 2’:6’,2’’-terpyridine: protonation and substituent effects
Eur. J. Org. Chem., 2008, 3569.

11) J. E. Beves, E. C. Constable, S. Decurtins, E. L. Dunphy, C. E. Housecroft, T. D. Keene, M. Neuburger, S. Schaffner
Homoleptic metal complexes of 4’-(5-pyrimidinyl)-2,2’:6’,2’’-terpyridine: tetrafurcated expanded ligands
CrystEngComm, 2008, 10, 986.

10) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner
A pyrazolyl-terminated 2,2’:6’,2’’-terpyridine ligand: iron(II), ruthenium(II) and palladium(II) complexes of 4’-(3,5-dimethylpyrazol-1-yl)-2,2’:6’,2’’-terpyridine
Polyhedron, 2008, 27, 2395.

9) J. E. Beves, D. J. Bray, J. K. Clegg, E. C. Constable, C. E. Housecroft, K. A. Jolliffe, C. J. Kepert, L. F. Lindoy, M. Neuburger, D. J. Price, S. Schaffner, F. Schaper
Expanding the 4,4′-bipyridine ligand: structural variation in {M(pytpy)2}2+ complexes (pytpy = 4′-(4-pyridyl)-2,2′:6′,2″-terpyridine, M = Fe, Ni, Ru) and assembly of the hydrogen-bonded, one-dimensional polymer {[Ru(pytpy)(Hpytpy)]}n3n
Inorg. Chim. Acta, 2008, 361, 2582.

8) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner
A one-dimensional copper(II) coordination polymer containing [Fe(pytpy)2]2+ (pytpy = 4-(4-pyridyl)-2,2’:6’,2’’-terpyridine) as an expanded 4,4-bipyridine ligand: a hydrogen-bonded network penetrated by rod-like polymers
CrystEngComm, 2008, 10, 344.

7) J. E. Beves, E. L. Dunphy, E. C. Constable, C. E. Housecroft, C. J. Kepert, M. Neuburger, D. J. Price, S. Schaffner.
Vectorial property dependence in bis{4′-(n-pyridyl)-2,2′:6′,2″-terpyridine}iron(II) and ruthenium(II) complexes with n = 2, 3 and 4
Dalton Trans., 2008, 386.

2007:

6) J. E. Beves, E. C. Constable, C. E. Housecroft, C. J. Kepert, M. Neuburger, D. J. Price, S. Schaffner.
The conjugate acid of bis{4′-(4-pyridyl)-2,2′:6′,2″-terpyridine}iron(II) as a self-complementary hydrogen-bonded building block
CrystEngComm 2007, 9, 1073.

5) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner
A palladium(II) complex of 4′-(4-pyridyl)-2,2′:6′,2″-terpyridine : lattice control through an interplay of stacking and hydrogen bonding effects
Inorg. Chem. Commun., 2007, 10, 1185.

4) J. E. Beves, E. C. Constable, C. E. Housecroft, C. J. Kepert, D. J. Price
The first example of a coordination polymer from the expanded 4,4′-bipyridine ligand [Ru(pytpy)2]2+ (pytpy = 4′-(4-pyridyl)-2,2′:6′,2”-terpyridine
CrystEngComm, 2007, 9, 456.

3) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner, E. J. Shardlow
[n + n]-Heterometallomacrocyclic complexes (n ≥  2) prepared from platinum(II)-centred ditopic 2,2′:6′,2”-terpyridine ligands: dimensional cataloguing by pulsed-field gradient spin-echo NMR spectroscopy
Dalton Trans. 2007, 1593.

2006:

2) J. E. Beves, E. C. Constable, C. E. Housecroft, M. Neuburger, S. Schaffner
4′-Chloro-2,2′:6′,2”-terpyridine.
Acta Cryst., Sec. E:, 2006, E62, o2497.

Pre-PhD:

1) J. E. Beves, B. E. Chapman, P. W. Kuchel, L. F. Lindoy, J. McMurtrie, M. McPartlin, P. Thordarson, G. Wei
New discrete metallocycles incorporating palladium(II) and platinum(II) corners and dipyridyldibenzotetraaza[14]annulene side units
Dalton Trans, 2006, 744.

Advertisements