CuTi-oxo clusters functionalized by - generated 2,2'-biphenolate ligands from the oxidative coupling of phenols.

Dalton Trans

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P. R. China.

Published: February 2023

Herein, we report a twisted cubic Cu(I)Ti(IV)-oxo cluster stabilized by - formed 2,2'-biphenolate ligands from the oxidative coupling of phenols. The 2,2'-biphenolate-functionalized Cu(I)Ti(IV)O cluster shows short Cu⋯C contacts and exhibits smaller HOMO-LUMO gaps than those of reported Ti(IV)O.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d2dt03756dDOI Listing

Publication Analysis

Top Keywords

22'-biphenolate ligands
8
ligands oxidative
8
oxidative coupling
8
coupling phenols
8
cuti-oxo clusters
4
clusters functionalized
4
functionalized generated
4
generated 22'-biphenolate
4
phenols report
4
report twisted
4

Similar Publications

Poly[di-aqua-[μ-1,4-bis-(pyridin-3-ylmeth-yl)piperazine][μ-4-(2-carboxyl-atoeth-yl)benzoato]cobalt(II)].

IUCrdata

December 2024

E-35 Holmes Hall, Michigan State University, Lyman Briggs College, 919 E. Shaw Lane, East Lansing, MI 48825, USA.

A layered cobalt coordination polymer containing both 4-(2-carboxyl-atoeth-yl)benzoate (ceb) and 1,4-bis-(3-pyridyl-meth-yl)piperazine (3-bpmp) ligands, [Co(CHO)(CHN)(HO)] or [Co(ceb)(3-bpmp)(HO)] , was isolated and structurally characterized by single-crystal X-ray diffraction. Chain-like [Co(ceb)(HO)] units are oriented parallel to [101]. These are connected into (4,4)-grid coordination polymer layers by tethering 3-bpmp ligands.

View Article and Find Full Text PDF

Optimized BCMA/CS1 bispecific TRuC-T cells secreting IL-7 and CCL21 robustly control multiple myeloma.

Front Immunol

December 2024

Key Laboratory of Laboratory Medicine, Ministry of Education, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China.

Introduction: Challenges remain in reducing antigen escape and tumor recurrence while CAR-T cell therapy has substantially improved outcomes in the treatment of multiple myeloma. T cell receptor fusion construct (TRuC)-T cells, which utilize intact T cell receptor (TCR)-CD3 complex to eliminate tumor cells in a non-major histocompatibility complex (MHC)-restricted manner, represent a promising strategy. Moreover, interleukin-7 (IL-7) is known to enhance the proliferation and survival of T cells.

View Article and Find Full Text PDF

Background: Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer, with the worst prognosis among all subtypes. The impact of distinct cell subpopulations within the tumor microenvironment (TME) on TNBC patient prognosis has yet to be clarified.

Methods: Utilizing single-cell RNA sequencing (scRNA-seq) integrated with bulk RNA sequencing (bulk RNA-seq), we applied Cox regression models to compute hazard ratios, and cross-validated prognostic scoring using a GLMNET-based Cox model.

View Article and Find Full Text PDF

CD28 shapes T cell receptor signaling by regulating Lck dynamics and ZAP70 activation.

Front Immunol

December 2024

Laboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States.

Introduction: T cell activation requires T cell receptor (TCR) engagement by its specific ligand. This interaction initiates a series of proximal events including tyrosine phosphorylation of the CD3 and TCRζ chains, recruitment, and activation of the protein tyrosine kinases Lck and ZAP70, followed by recruitment of adapter and signaling proteins. CD28 co-stimulation is also required to generate a functional immune response.

View Article and Find Full Text PDF

Based on their ability to canvas vast genetic or chemical space at low cost and high speed, DNA-encoded libraries (DEL) have served to enable both genomic and small molecule discovery. Current DEL chemical library screening approaches focus primarily on target-based affinity or activity. Here we describe an approach to record the phenotype-based activity of DNA-encoded small molecules on their cognate barcode in living cells.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!