2009
DOI: 10.1039/b812807c
|View full text |Cite
|
Sign up to set email alerts
|

Controlling the dimensionalities and structures of homochiral Zn(ii) and Cd(ii) compounds of N-(p-tosyl)-S-carboxymethyl-l-cysteinevia tuning the connecting modes of metal ions and chiral linkers by different kinds of ancillary ligands

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
16
0

Year Published

2009
2009
2025
2025

Publication Types

Select...
8

Relationship

3
5

Authors

Journals

citations
Cited by 46 publications
(17 citation statements)
references
References 78 publications
1
16
0
Order By: Relevance
“…1. It is shown that N1, C1, C2, N3 and C15 are nearly located in one plane and the N1-C1, C1-C2, C2-N3, N3-C15 and C15-N1 bond lengths and the corresponding bond angles (Table 4) in the ring are comparable to those in the imidazole ring reported [23][24][25][26]. This confirms the existence of the imidazole ring in compound L 2 .…”
Section: 2supporting
confidence: 84%
“…1. It is shown that N1, C1, C2, N3 and C15 are nearly located in one plane and the N1-C1, C1-C2, C2-N3, N3-C15 and C15-N1 bond lengths and the corresponding bond angles (Table 4) in the ring are comparable to those in the imidazole ring reported [23][24][25][26]. This confirms the existence of the imidazole ring in compound L 2 .…”
Section: 2supporting
confidence: 84%
“…A mixture of S-carboxymethyl-N-p-tosyl-l-cysteine (0.0667 g, 0.2 mmol), prepared according to the literature method of Chen et al (2009), 4,4 0 -bipyridine (0.0312 g, 0.2 mmol), Mn(CH 3 COO) 2 Á4H 2 O (0.0490 g, 0.2 mmol) and water (8 ml) was sealed in a 23 ml Teflonlined autoclave, heated at 353 K for 6 d and cooled over a period of 48 h. Yellow crystals of (I) were collected in a yield of 63% (0.0706 g). H atoms of amine groups and water molecules were located in a difference Fourier map and allowed for as riding on their parent atoms [U iso (H) = 1.5U eq (O) and 1.2U eq (N)].…”
Section: Methodsmentioning
confidence: 99%
“…Because Sr II , Zn II , and Cd II ions are difficult to oxidize or to reduce due to their features of electronic configuration, the emission bands of complexes 1-3 are neither metal-to-ligand charge transfer nor ligand-to-metal charge transfer in nature. [40][41][42][43] So, the emission of 1-3 may be attributed to the ligand-to-ligand charge transfer. The different emission bands of the three polymers may be attributed to the coordination diversities of the metal centres and the rigid differences of coordination modes.…”
Section: Photoluminescence Propertiesmentioning
confidence: 99%
“…[38][39][40][41] Hence, the solid-state luminescence properties of 1-3 were studied at room temperature (Fig. 6).…”
Section: Photoluminescence Propertiesmentioning
confidence: 99%