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1.
Photochem Photobiol Sci ; 18(11): 2782-2791, 2019 Nov 01.
Article in English | MEDLINE | ID: mdl-31620765

ABSTRACT

The development of water oxidation catalysts based on Earth-abundant metals that can function at neutral pH remains a basic chemical challenge. Here, we report that salophen complexes with Ni(ii), Cu(ii), and Mn(ii) can catalyse photochemical water oxidation to molecular oxygen in the presence of [Ru(bpy)3]2+ as a photosensitizer and Na2S2O8 as an oxidant in phosphate buffer of pH 7.0. Experimental results including CV, SEM, EDS, ESI-MS, and DLS measurements on the metal salophen complex-catalysed water oxidation to oxygen suggest that the catalytic activity of the catalysts is molecular in origin.

2.
Acta Crystallogr Sect E Struct Rep Online ; 66(Pt 1): o241, 2009 Dec 24.
Article in English | MEDLINE | ID: mdl-21580122

ABSTRACT

In the title compound, C(16)H(25)N(3)OS, the thio-semicarbazone group adopts an E configuration with respect to the C=N bond and is almost coplanar with the benzene ring, forming a dihedral angle of 9.3 (1)°. In the crystal packing, the mol-ecules lie along the a axis in an anti-parallel arrangement and are held in place by van der Waals inter-actions. As a consequence, there is relatively low anisotropic thermal motion in the terminal atoms of the n-octyl chain.

3.
Acta Crystallogr Sect E Struct Rep Online ; 64(Pt 4): m518-9, 2008 Mar 05.
Article in English | MEDLINE | ID: mdl-21201987

ABSTRACT

In the title Zn(II) complex, [Zn(C(17)H(15)N(2)S(2))(2)], the Zn(II) atom lies on a twofold rotation axis. It exists in a tetra-hedral geometry, chelated by two deprotonated Schiff base ligands. The dihedral angle between each ligand is 71.48 (8)°. Mol-ecules are connected by weak C-H⋯S inter-molecular inter-actions into chains along the c axis. The crystal structure is further stabilized by C-H⋯π inter-actions involving the phenyl ring of the 3-phenyl-prop-2-enyl-idene unit.

4.
Acta Crystallogr C ; 57(Pt 10): 1207-8, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11600787

ABSTRACT

The title compound, C(7)H(8)N(2)O(2), is monoclinic (space group P2(1)/n) at 295 (2) K with Z' = 2. The two types of molecule form independent C(7) chains, and the structure is related to that of the low-temperature triclinic polymorph, where Z' = 4 in P1, by a simple displacive transformation.

5.
Acta Crystallogr C ; 57(Pt 8): 914-7, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11498611

ABSTRACT

In ferrocene-1,1'-diylbis(diphenylmethanol)-4,4'-ethylenedipyridine (1/1), [Fe(C(18)H(15)O)(2)].C(12)H(12)N(2), there is an intramolecular O-H...O hydrogen bond in the ferrocenediol component and a single O-H...N hydrogen bond linking the two components into a finite monomeric adduct. Ferrocene-1,1'-diylbis(diphenylmethanol)-ethylenediamine (1/1), [Fe(C(18)H(15)O)(2)].C(2)H(8)N(2), crystallizes with Z' = 2 in space group P1, and there are two independent four-component aggregates in the structure, both of which are centrosymmetric. In the first type of aggregate, the molecular components are linked by O-H...N and N-H...O hydrogen bonds, in which both diamine N atoms participate; in the second type of aggregate, the diamine component is disordered over two sets of sites, but only one N atom is involved in the hydrogen bonding.

6.
Acta Crystallogr C ; 57(Pt 8): 922-3, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11498613

ABSTRACT

In the title compound, [Na(C(2)H(3)N(2)O(3))], the Na(+) cation lies on a centre of inversion in space group P2(1)/m and all the atoms of the anion lie on a mirror plane. Na is octahedrally coordinated by four O and two N atoms from six different anions and each anion is coordinated to six different Na(+) cations, forming chains of confacial octahedra which link the anion layers. Within these layers, the individual anions are linked by both O-H...O and C-H...O hydrogen bonds.

7.
Acta Crystallogr C ; 57(Pt 6): 683-6, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11408670

ABSTRACT

The title compound, [Ni2(C8H4O4)(C10H24N4)2(H2O)2](ClO4)2, contains two independent octahedral Ni(II) centres with trans-NiN4O2 chromophores. The bridging benzenedicarboxylate ligand is bonded to the two Ni atoms, each via one O atom of each carboxylate, while the other O atom participates in an intramolecular N-H...O hydrogen bond, forming an S(6) motif. The cations are linked to the perchlorate anions via O-H...O and N-H...O hydrogen bonds [O...O 2.904 (6) and 2.898 (6) A; O-H...O 158 (6) and 165 (6) degrees; N...O 3.175 (7) and 3.116 (7) A; N-H...O 168 and 166 degrees ] to form molecular ladders. These ladders are linked by further O-H...O and N-H...O hydrogen bonds [O...O 2.717 (6) and 2.730 (5) A; O-H...O 170 (4) and 163 (6) degrees; N...O 3.373 (7) and 3.253 (7) A; N-H...O 163 and 167 degrees ] to form a continuous three-dimensional framework. The perchlorate anions both participate in three hydrogen bonds, and both are thus fully ordered.

8.
Acta Crystallogr C ; 57(Pt 6): 687-9, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11408671

ABSTRACT

In the title compound, 2[Fe(C5H5)(C6H5O2)].C6H12N2, the molecular components are linked into finite three-component aggregates by strong O-H...N hydrogen bonds [O.N 2.578 (4) and 2.604 (5) A; O-H...N 170 (5) and 174 (6) degrees ]; these aggregates are further linked by C-H...O hydrogen bonds [C...O 3.327 (5)-3.401 (5) A; C-H...O 149-157 degrees ] into continuous sheets in the form of (6,3) nets.

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